Allele Registry

Canonical Allele Identifier: PA115066

Gene: HPD HGNC NCBI

ClinVar Allele:

16615

ClinVar RCV:

RCV000001642

RCV000386406

RCV000953322

RCV001091863

RCV003488319

RCV003964786

ClinVar Variation:

1576

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165464.1:p.Ile296Met	CA115065 NM_001171993.2:c.888C>G