Canonical Allele Identifier: PA100081
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 10744
ClinVar RCV Id: RCV000011492
ClinVar Variation Id: 245750
ClinVar RCV Id: RCV000235836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Gly361Arg
CA021360
NM_000169.3:c.1081G>C
CA10584626
NM_000169.3:c.1081G>A