Allele Registry

Canonical Allele Identifier: PA2826559382

Gene: TP53 HGNC NCBI

ClinVar Allele:

420662

ClinVar RCV:

RCV000492685

RCV000799619

RCV002289662

ClinVar Variation:

428863

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Asp109Tyr	CA397842304 NM_001276695.3:c.325G>T