Allele Registry

Canonical Allele Identifier: PA102779

Gene: HGD HGNC NCBI

ClinVar RCV:

RCV000003323

RCV002279945

RCV002287319

ClinVar Variation:

3173

HGVS (amino-acid)	Matching Registered Transcripts
NP_000178.2:p.Met368Val	CA340048 NM_000187.4:c.1102A>G