Canonical Allele Identifier: PA107169
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 946154
ClinVar RCV Id: RCV001216955 RCV001700721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.His342Tyr
CA414519008
NM_000202.8:c.1024C>T