ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2826559654
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
216077
ClinVar RCV Id:
RCV000198789
RCV000418938
RCV000423911
RCV000434089
RCV000421097
RCV000421751
RCV000439388
RCV000441624
RCV000434805
RCV000442071
RCV000429852
RCV000436603
RCV000438726
RCV000419621
RCV000428484
RCV000429211
RCV000437301
RCV000487386
RCV000785324
RCV001024600
RCV001271054
RCV002288812
RCV003474953
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263624.1:p.Ile156Thr
CA002232
NM_001276695.3:c.467T>C