Canonical Allele Identifier: PA100618
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 496868
ClinVar RCV Id: RCV000593774 RCV003509574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Trp287Cys
CA413922716
NM_000169.3:c.861G>T
CA413922719
NM_000169.3:c.861G>C