Canonical Allele Identifier: PA2827646841
Gene: ALG9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339348.1:p.Asn390Ser
CA6274357
NM_001352419.1:c.1169A>G