Canonical Allele Identifier: PA658669978
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 449348
ClinVar RCV Id: RCV000520378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Ile230Phe
CA414522170
NM_000202.8:c.688A>T