Canonical Allele Identifier: PA2826562681
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Pro159Leu
CA397835952
NM_001276697.3:c.476C>T