Canonical Allele Identifier: PA2579935657
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406606
ClinVar RCV Id: RCV000462657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Asp184Gly
CA16615998
NM_000546.6:c.551A>G