Allele Registry

Canonical Allele Identifier: PA102322

Gene: HGD HGNC NCBI

ClinVar RCV:

RCV000169601

ClinVar Variation:

189173

HGVS (amino-acid)	Matching Registered Transcripts
NP_000178.2:p.Arg225His	CA277989 NM_000187.4:c.674G>A