Canonical Allele Identifier: PA916035342
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_001339351.1:p.Tyr91Cys
CA252862
NM_001352422.2:c.272A>G