Canonical Allele Identifier: PA2825081808
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1492947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Ala317Asp
CA10537544
NM_000202.8:c.950C>A