Canonical Allele Identifier: PA2826033209
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 2138748
ClinVar RCV Id: RCV003066392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.His245Arg
CA414519820
NM_001166550.4:c.734A>G