Canonical Allele Identifier: PA891846410
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 589539
ClinVar RCV Id: RCV000719615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Asn181Ser
CA414522526
NM_000202.8:c.542A>G