Allele Registry

Canonical Allele Identifier: PA102963

Gene: HGD HGNC NCBI

ClinVar RCV:

RCV000003316

ClinVar Variation:

3166

HGVS (amino-acid)	Matching Registered Transcripts
NP_000178.2:p.Val300Gly	CA340043 NM_000187.4:c.899T>G