Canonical Allele Identifier: PA2826566960
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ser144Leu
CA397841206
NM_001276761.3:c.431C>T