Canonical Allele Identifier: PA2826033066
Gene: IDS HGNC NCBI
ClinVar Allele:
98528
ClinVar RCV:
RCV000178730
ClinVar Variation:
92620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Leu106Ser
CA220495
NM_001166550.4:c.317T>C