Allele Registry

Canonical Allele Identifier: PA645386118

Gene: PRCD HGNC NCBI

ClinVar Variation Id: 325472

HGVS (amino-acid)	Matching Registered Transcripts
NP_001071088.1:p.Arg17Cys	CA8787804 NM_001077620.3:c.49C>T