Canonical Allele Identifier: PA2827646942
Gene: ALG9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2048922
ClinVar RCV Id: RCV002932129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339349.1:p.Asn383Ser
CA6274357
NM_001352420.2:c.1148A>G