Canonical Allele Identifier: PA2829630466
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 2807843
ClinVar RCV Id: RCV003622535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006114.1:p.Thr130Ala
CA414525751
NM_006123.5:c.388A>G