Canonical Allele Identifier: PA2580449125
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_079016.2:p.Asn561Ser
CA6274357
NM_024740.2:c.1682A>G