Canonical Allele Identifier: PA645469588
Gene: HGD HGNC NCBI

Linked Data

ClinVar Variation Id: 342751
ClinVar RCV Id: RCV000359600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000178.2:p.Pro103Thr
CA2560267
NM_000187.4:c.307C>A