Canonical Allele Identifier: PA100031
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 10722
ClinVar RCV Id: RCV000011469 RCV000723846
ClinVar Variation Id: 198053
ClinVar RCV Id: RCV000179268 RCV000780293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Gly328Arg
CA022255
NM_000169.3:c.982G>A
CA022260
NM_000169.3:c.982G>C