Canonical Allele Identifier: PA2741813073
Gene: HGD HGNC NCBI

Linked Data

ClinVar Variation Id: 2559813
ClinVar RCV Id: RCV003309513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000178.2:p.Ser67Pro
CA2560307
NM_000187.4:c.199T>C