Canonical Allele Identifier: PA102599
Gene: HGD HGNC NCBI

Linked Data

ClinVar Variation Id: 3168
ClinVar RCV Id: RCV000003318 RCV001725928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000178.2:p.Gly161Arg
CA340044
NM_000187.4:c.481G>A
CA354077164
NM_000187.4:c.481G>C