Canonical Allele Identifier: PA2499229615
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 997009
ClinVar RCV Id: RCV001564020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Pro469Leu
CA414518164
NM_000202.8:c.1406C>T