Canonical Allele Identifier: PA2573184267
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1420774
ClinVar RCV Id: RCV001923583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Thr28Ser
CA414526083
NM_001166550.4:c.83C>G
CA414526091
NM_001166550.4:c.82A>T