Canonical Allele Identifier: PA2825081543
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1478222
ClinVar RCV Id: RCV002018949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Ser152Arg
CA337036612
NM_000202.8:c.456C>G
CA414523140
NM_000202.8:c.456C>A
CA414523152
NM_000202.8:c.454A>C