Canonical Allele Identifier: PA2827646942
Gene: ALG9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339349.1:p.Asn383Ser
CA6274357
NM_001352420.2:c.1148A>G