Canonical Allele Identifier: PA2579952269
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 660046
ClinVar RCV Id: RCV000817167
ClinVar Variation Id: 926470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.His297Gln
CA397836436
NM_000546.6:c.891C>G
CA397836439
NM_000546.6:c.891C>A