Canonical Allele Identifier: PA2827647032
Gene: ALG9 HGNC NCBI

Linked Data

ClinVar Variation Id: 96135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339351.1:p.Ala36Pro
CA223762
NM_001352422.2:c.106G>C