Canonical Allele Identifier: PA106666
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 10500
ClinVar RCV Id: RCV000011246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Arg468Leu
CA121099
NM_000202.8:c.1403G>T