Canonical Allele Identifier: PA252863
Gene: ALG9 HGNC NCBI

Linked Data

ClinVar Variation Id: 3749
ClinVar RCV Id: RCV000003947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079016.2:p.Tyr287Cys
CA252862
NM_024740.2:c.860A>G