Canonical Allele Identifier: PA2826567879
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Lys333Arg
CA10580901
NM_001276761.3:c.998A>G