Allele Registry

Canonical Allele Identifier: PA916039088

Gene: PRKCD HGNC NCBI

ClinVar RCV:

RCV000144966

RCV003105796

ClinVar Variation:

157675

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341605.1:p.Arg633Trp	CA171034 NM_001354676.2:c.1897C>T