Allele Registry

Canonical Allele Identifier: PA916035342

Gene: ALG9 HGNC NCBI

ClinVar Allele:

18788

ClinVar RCV:

RCV000003947

ClinVar Variation:

3749

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339351.1:p.Tyr91Cys	CA252862 NM_001352422.2:c.272A>G