Canonical Allele Identifier: PA2741926438
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 3000159
ClinVar RCV Id: RCV003857334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006114.1:p.Asn325Ser
CA10537538
NM_006123.5:c.974A>G