Canonical Allele Identifier: PA2826033337
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 10497
ClinVar RCV Id: RCV000011243 RCV000180471 RCV000723439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Arg378Trp
CA340991
NM_001166550.4:c.1132C>T