Allele Registry

Canonical Allele Identifier: PA2826562697

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV003177183

ClinVar Variation:

2450758

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Asp165Glu	CA397835829 NM_001276697.3:c.495T>A CA397835833 NM_001276697.3:c.495T>G