ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA108597
Gene: PIK3CA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
13652
ClinVar RCV Id:
RCV000014623
RCV000014624
RCV000014626
RCV000014627
RCV000014628
RCV000014622
RCV000024621
RCV000154516
RCV000201231
RCV000420562
RCV000419938
RCV000426498
RCV000426614
RCV000437153
RCV000432506
RCV000421855
RCV000422442
RCV000442731
RCV000428372
RCV000442164
RCV000431232
RCV000437782
RCV000438435
RCV000443546
RCV000487449
RCV000425956
RCV000430589
RCV000432543
RCV000433127
RCV000436234
RCV000437287
RCV000442736
RCV000709691
RCV001092442
RCV001255686
RCV001327968
RCV001526648
RCV001705589
RCV001705590
RCV001807727
RCV001728091
RCV001729349
RCV001730472
RCV001836707
RCV003128082
RCV003325939
RCV002508124
RCV004527290
RCV004527291
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_006209.2:p.His1047Arg
CA123326
NM_006218.4:c.3140A>G