Canonical Allele Identifier: PA131279
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 42462
ClinVar RCV Id: RCV000035311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Leu243Phe
CA022020
NM_000169.3:c.729G>C
CA413924418
NM_000169.3:c.729G>T