Allele Registry

Canonical Allele Identifier: PA645390060

Gene: ALG9 HGNC NCBI

ClinVar Allele:

324362

ClinVar RCV:

RCV000274374

RCV001850600

ClinVar Variation:

302425

HGVS (amino-acid)	Matching Registered Transcripts
NP_079016.2:p.Arg554Trp	CA6274361 NM_024740.2:c.1660C>T