Allele Registry

Canonical Allele Identifier: PA915979529

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000824567

RCV002372364

ClinVar Variation:

666137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119586.1:p.Ala307Val	CA397836165 NM_001126114.3:c.920C>T