Canonical Allele Identifier: PA122165
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Val157Phe
CA000222
NM_001126112.3:c.469G>T