Canonical Allele Identifier: PA102368
Gene: HGD HGNC NCBI

Linked Data

ClinVar Variation Id: 370939
ClinVar RCV Id: RCV000412076 RCV001726153
JSON-LD

Amino-acid Alleles

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