Canonical Allele Identifier: PA2827647151
Gene: ALG9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339352.1:p.Pro232Arg
CA6274441
NM_001352423.2:c.695C>G