Canonical Allele Identifier: PA2580108708
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 2047467
ClinVar RCV Id: RCV002904325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Asn537Ser
CA414517698
NM_000202.8:c.1610A>G