Canonical Allele Identifier: PA2826564275
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376598
ClinVar RCV Id: RCV000420461 RCV000425222 RCV000425855 RCV000430671 RCV000435260 RCV000435460 RCV000438306 RCV000443062 RCV000443210 RCV001027160
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Phe111Val
CA16603020
NM_001276699.3:c.331T>G