ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2826563064
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376609
ClinVar RCV Id:
RCV000419091
RCV000418067
RCV000419301
RCV000422109
RCV000422797
RCV000424599
RCV000424807
RCV000427824
RCV000429415
RCV000430449
RCV000433706
RCV000434154
RCV000433494
RCV000435925
RCV000434865
RCV000440508
RCV000440898
RCV000445154
RCV000444321
RCV000564826
RCV000695193
RCV001575036
RCV004022218
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263627.1:p.His20Asn
CA16603030
NM_001276698.3:c.58C>A