Canonical Allele Identifier: PA2825608211
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 573679
ClinVar RCV Id: RCV000695405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Glu221Ala
CA397839870
NM_001126114.3:c.662A>C