Canonical Allele Identifier: PA102690
Gene: HGD HGNC NCBI

Linked Data

ClinVar Variation Id: 3172
ClinVar RCV Id: RCV000003322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000178.2:p.His371Arg
CA277917
NM_000187.4:c.1112A>G