Allele Registry

Canonical Allele Identifier: PA171035

Gene: PRKCD HGNC NCBI

ClinVar RCV:

RCV000144966

RCV003105796

ClinVar Variation:

157675

HGVS (amino-acid)	Matching Registered Transcripts
NP_006245.2:p.Arg614Trp	CA171034 NM_006254.4:c.1840C>T