Canonical Allele Identifier: PA2825081438
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 996920
ClinVar RCV Id: RCV001291744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Cys84Trp
CA414526933
NM_000202.8:c.252C>G