Canonical Allele Identifier: PA100021
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 10740
ClinVar RCV Id: RCV000011488 RCV000723545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Gly328Ala
CA022267
NM_000169.3:c.983G>C