Allele Registry

Canonical Allele Identifier: PA100021

Gene: GLA HGNC NCBI

ClinVar RCV:

RCV000011488

RCV000723545

ClinVar Variation:

10740

HGVS (amino-acid)	Matching Registered Transcripts
NP_000160.1:p.Gly328Ala	CA022267 NM_000169.3:c.983G>C