Allele Registry

Canonical Allele Identifier: PA102368

Gene: HGD HGNC NCBI

ClinVar RCV:

RCV000412076

RCV001726153

ClinVar Variation:

370939

HGVS (amino-acid)	Matching Registered Transcripts
NP_000178.2:p.Arg53Gln	CA2560335 NM_000187.4:c.158G>A