Allele Registry

Canonical Allele Identifier: PA2826561789

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV003177183

ClinVar Variation:

2450758

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Asp285Glu	CA397835829 NM_001276696.3:c.855T>A CA397835833 NM_001276696.3:c.855T>G