Canonical Allele Identifier: PA2499229616
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1186178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Pro473Ser
CA414518143
NM_000202.8:c.1417C>T