Canonical Allele Identifier: PA2826033171
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1001594
ClinVar RCV Id: RCV001297916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Tyr210Asp
CA414520445
NM_001166550.4:c.628T>G