Canonical Allele Identifier: PA2825081795
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 997010
ClinVar RCV Id: RCV001564021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Asp308Gly
CA414520293
NM_000202.8:c.923A>G