Canonical Allele Identifier: PA2825081542
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 996749
ClinVar RCV Id: RCV001563681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Ser152Asn
CA414523145
NM_000202.8:c.455G>A