Canonical Allele Identifier: PA2826562822
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Ala196Gly
CA397832140
NM_001276697.3:c.587C>G