Canonical Allele Identifier: PA2499229610
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 996921
ClinVar RCV Id: RCV001291745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Ser349Arg
CA414518948
NM_000202.8:c.1047C>G
CA414518949
NM_000202.8:c.1047C>A
CA414518954
NM_000202.8:c.1045A>C