Canonical Allele Identifier: PA100447
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 495691
ClinVar RCV Id: RCV000586514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Pro409Ala
CA413919170
NM_000169.3:c.1225C>G