Allele Registry

Canonical Allele Identifier: PA916039083

Gene: PRKCD HGNC NCBI

ClinVar Allele:

167523

ClinVar RCV:

RCV000144965

ClinVar Variation:

157674

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341605.1:p.Gly529Ser	CA171032 NM_001354676.2:c.1585G>A