Canonical Allele Identifier: PA169049
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Val11Met
CA000176
NM_001126116.1:c.31G>A