Canonical Allele Identifier: PA645436112
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Val40Phe
CA397841576
NM_001126117.1:c.118G>T