Allele Registry

Canonical Allele Identifier: PA2827916599

Gene: PRKCD HGNC NCBI

ClinVar RCV:

RCV000144965

ClinVar Variation:

157674

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341609.1:p.Gly510Ser	CA171032 NM_001354680.2:c.1528G>A