Canonical Allele Identifier: PA100595
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 501332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Trp236Cys
CA353009
NM_000169.3:c.708G>C
CA413924684
NM_000169.3:c.708G>T