Canonical Allele Identifier: PA122170
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Val25Phe
CA000222
NM_001126117.1:c.73G>T