Canonical Allele Identifier: PA100138
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 2138671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.His46Pro
CA413937084
NM_000169.3:c.137A>C