Allele Registry

Canonical Allele Identifier: PA915984886

Gene: HPD HGNC NCBI

ClinVar RCV:

RCV000001639

RCV001297386

RCV001731268

ClinVar Variation:

1573

HGVS (amino-acid)	Matching Registered Transcripts
NP_002141.2:p.Tyr160Cys	CA115056 NM_002150.3:c.479A>G