Canonical Allele Identifier: PA2741813123
Gene: HGD HGNC NCBI

Linked Data

ClinVar Variation Id: 2627689
ClinVar RCV Id: RCV003388983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000178.2:p.Gly205Asp
CA2560145
NM_000187.4:c.614G>A