Canonical Allele Identifier: PA2825081791
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1509067
ClinVar RCV Id: RCV002017626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Ser305Pro
CA414520359
NM_000202.8:c.913T>C