Canonical Allele Identifier: PA2825607397
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 444396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Met160Val
CA397841976
NM_001126114.3:c.478A>G