Canonical Allele Identifier: PA107221
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 92620
ClinVar RCV Id: RCV000178730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Leu196Ser
CA220495
NM_000202.8:c.587T>C