Canonical Allele Identifier: PA2573164349
Gene: HGD HGNC NCBI

Linked Data

ClinVar Variation Id: 1410610
ClinVar RCV Id: RCV001928123 RCV002555792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000178.2:p.Gly323Arg
CA2560007
NM_000187.4:c.967G>A
CA354073445
NM_000187.4:c.967G>C