Canonical Allele Identifier: PA2826033204
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1459022
ClinVar RCV Id: RCV001949645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Ser243Trp
CA414519855
NM_001166550.4:c.728C>G