Canonical Allele Identifier: PA915979529
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 666137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ala307Val
CA397836165
NM_001126114.3:c.920C>T