Allele Registry

Canonical Allele Identifier: PA915984867

Gene: HPD HGNC NCBI

ClinVar RCV:

RCV000988927

RCV001518865

RCV001702760

RCV001805956

ClinVar Variation:

802899

HGVS (amino-acid)	Matching Registered Transcripts
NP_002141.2:p.Thr33Ala	CA6839814 NM_002150.3:c.97A>G