Allele Registry

Canonical Allele Identifier: PA100321

Gene: GLA HGNC NCBI

ClinVar Variation Id: 10763

ClinVar RCV Id: RCV000011510

ClinVar Variation Id: 1396452

ClinVar RCV Id: RCV001919968

HGVS (amino-acid)	Matching Registered Transcripts
NP_000160.1:p.Met296Ile	CA022146 NM_000169.3:c.888G>A CA413922414 NM_000169.3:c.888G>T CA413922418 NM_000169.3:c.888G>C