Canonical Allele Identifier: PA100098
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 177834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Gly373Ser
CA021403
NM_000169.3:c.1117G>A