Canonical Allele Identifier: PA356954
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 221970
ClinVar RCV Id: RCV000207419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Asp45His
CA356953
NM_000202.8:c.133G>C