Canonical Allele Identifier: PA645436017
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 246069
ClinVar RCV Id: RCV000235861
ClinVar Variation Id: 1361331
ClinVar RCV Id: RCV001874295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Tyr327Ter
CA645587349
NM_001126114.3:c.980_981insAA