Allele Registry

Canonical Allele Identifier: PA2825454961

Gene: ALG9 HGNC NCBI

ClinVar Allele:

324362

ClinVar RCV:

RCV000274374

RCV001850600

ClinVar Variation:

302425

HGVS (amino-acid)	Matching Registered Transcripts
NP_001071158.1:p.Arg547Trp	CA6274361 NM_001077690.1:c.1639C>T