Canonical Allele Identifier: PA2825611490
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 496049
ClinVar RCV Id: RCV000588420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Leu157Val
CA397836620
NM_001126115.1:c.469C>G