Allele Registry

Canonical Allele Identifier: PA2826955168

Gene: PRKCD HGNC NCBI

ClinVar RCV:

RCV000144966

RCV003105796

ClinVar Variation:

157675

HGVS (amino-acid)	Matching Registered Transcripts
NP_001303256.1:p.Arg614Trp	CA171034 NM_001316327.2:c.1840C>T