Canonical Allele Identifier: PA106666
Gene: IDS HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Arg468Leu
CA121099
NM_000202.8:c.1403G>T