Canonical Allele Identifier: PA100555
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 10771
ClinVar RCV Id: RCV000011518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Thr410Ala
CA021462
NM_000169.3:c.1228A>G