Canonical Allele Identifier: PA266771
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 92541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Met42Thr
CA021500
NM_000169.3:c.125T>C