Canonical Allele Identifier: PA2741841120
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 2785080
ClinVar RCV Id: RCV003621834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Pro60Ser
CA414523186
NM_001166550.4:c.178C>T