Canonical Allele Identifier: PA100566
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 10728
ClinVar RCV Id: RCV000011475 RCV003137512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Trp162Arg
CA021748
NM_000169.3:c.484T>C
CA413929232
NM_000169.3:c.484T>A