Canonical Allele Identifier: PA658679191
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro82Ala
CA397845525
NM_001126114.3:c.244C>G