Canonical Allele Identifier: PA2826562934
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Gly230Arg
CA397830162
NM_001276697.3:c.688G>A
CA397830168
NM_001276697.3:c.688G>C