Canonical Allele Identifier: PA353259
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 217398
ClinVar RCV Id: RCV000209382 RCV000209767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Trp262Arg
CA353257
NM_000169.3:c.784T>C
CA413923929
NM_000169.3:c.784T>A