Canonical Allele Identifier: PA2579952065
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485027
ClinVar RCV Id: RCV000568377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Ala307Gly
CA397836168
NM_000546.6:c.920C>G