Canonical Allele Identifier: PA658679421
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Thr284Ser
CA397836761
NM_001126114.3:c.850A>T