Canonical Allele Identifier: PA102322
Gene: HGD HGNC NCBI

Linked Data

ClinVar Variation Id: 189173
ClinVar RCV Id: RCV000169601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000178.2:p.Arg225His
CA277989
NM_000187.4:c.674G>A