Canonical Allele Identifier: PA2826565638
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 573679
ClinVar RCV Id: RCV000695405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Glu182Ala
CA397839870
NM_001276760.3:c.545A>C