Allele Registry

Canonical Allele Identifier: PA2827916636

Gene: PRKCD HGNC NCBI

ClinVar RCV:

RCV000144966

RCV003105796

ClinVar Variation:

157675

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341609.1:p.Arg614Trp	CA171034 NM_001354680.2:c.1840C>T