Canonical Allele Identifier: PA2579952002
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1720175
ClinVar RCV Id: RCV002297978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Asn310Ile
CA397836112
NM_000546.6:c.929A>T