Canonical Allele Identifier: PA915989938
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 527323
ClinVar RCV Id: RCV000632181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Thr40Ile
CA414525737
NM_001166550.4:c.119C>T