Canonical Allele Identifier: PA100298
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 180842
ClinVar RCV Id: RCV000157900 RCV000627818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Met267Ile
CA022081
NM_000169.3:c.801G>A
CA413923762
NM_000169.3:c.801G>T
CA413923763
NM_000169.3:c.801G>C