Canonical Allele Identifier: PA2573061773
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1302719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Gly374Val
CA414518789
NM_000202.8:c.1121G>T