Allele Registry

Canonical Allele Identifier: PA147589

Gene: PRKCSH HGNC NCBI

ClinVar RCV:

RCV000080027

RCV000381668

RCV001537232

ClinVar Variation:

94079

HGVS (amino-acid)	Matching Registered Transcripts
NP_002734.2:p.Ala291Thr	CA147588 NM_002743.3:c.871G>A