Canonical Allele Identifier: PA2826566548
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ala35Val
CA000077
NM_001276761.3:c.104C>T