Canonical Allele Identifier: PA916012779
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 92622
ClinVar RCV Id: RCV000078368 RCV000205107 RCV000587097 RCV002311549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006114.1:p.Thr214Met
CA331784
NM_006123.5:c.641C>T