Canonical Allele Identifier: PA2827645911
Gene: ALG9 HGNC NCBI

Linked Data

ClinVar Variation Id: 96135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339340.1:p.Ala61Pro
CA223762
NM_001352411.2:c.181G>C