Canonical Allele Identifier: PA2573184269
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1447387
ClinVar RCV Id: RCV001979794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Tyr38Ser
CA414525798
NM_001166550.4:c.113A>C