Canonical Allele Identifier: PA2827646583
Gene: ALG9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339346.1:p.Pro444Arg
CA6274441
NM_001352417.1:c.1331C>G