Canonical Allele Identifier: PA100091
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 222145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Gly373Asp
CA352566
NM_000169.3:c.1118G>A