Allele Registry

Canonical Allele Identifier: PA2826562082

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000709405

RCV002289988

RCV002289989

ClinVar Variation:

584922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Asp49Gly	CA397840196 NM_001276697.3:c.146A>G