Canonical Allele Identifier: PA102912
Gene: HGD HGNC NCBI

Linked Data

ClinVar Variation Id: 2626821
ClinVar RCV Id: RCV003387458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000178.2:p.Trp60Gly
CA354081607
NM_000187.4:c.178T>G