Allele Registry

Canonical Allele Identifier: PA2826562086

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV003177174

ClinVar Variation:

2450746

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Arg50Ser	CA397840166 NM_001276697.3:c.150A>T CA397840167 NM_001276697.3:c.150A>C