Canonical Allele Identifier: PA096817
Gene: ALG9 HGNC NCBI
ClinVar Allele:
18788
ClinVar RCV:
RCV000003947
ClinVar Variation:
3749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071158.1:p.Tyr287Cys
CA252862
NM_001077690.1:c.860A>G