Canonical Allele Identifier: PA168220
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Val73Met
CA000075
NM_001126114.3:c.217G>A