Canonical Allele Identifier: PA2826033341
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 2230429
ClinVar RCV Id: RCV002717601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Pro379Arg
CA414518165
NM_001166550.4:c.1136C>G