Canonical Allele Identifier: PA2827646681
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_001339347.1:p.Tyr287Cys
CA252862
NM_001352418.1:c.860A>G