Canonical Allele Identifier: PA2829630383
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 988674
ClinVar RCV Id: RCV001290998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006114.1:p.Tyr103Asp
CA414526498
NM_006123.5:c.307T>G