Allele Registry

Canonical Allele Identifier: PA2826381111

Gene: HPGD HGNC NCBI

ClinVar Allele:

22956

ClinVar RCV:

RCV000008379

RCV000144084

RCV001781205

ClinVar Variation:

7917

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243230.1:p.Ala19Pro	CA119153 NM_001256301.1:c.55G>C