Canonical Allele Identifier: PA102537
Gene: HGD HGNC NCBI
ClinVar RCV:
RCV000409498
ClinVar Variation:
371502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000178.2:p.Glu401Gln
CA2559930
NM_000187.4:c.1201G>C