Allele Registry

Canonical Allele Identifier: PA252863

Gene: ALG9 HGNC NCBI

ClinVar Allele:

18788

ClinVar RCV:

RCV000003947

ClinVar Variation:

3749

HGVS (amino-acid)	Matching Registered Transcripts
NP_079016.2:p.Tyr287Cys	CA252862 NM_024740.2:c.860A>G