Canonical Allele Identifier: PA2741812050
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 2578164
ClinVar RCV Id: RCV003325763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000193.1:p.Val357Ala
CA337035861
NM_000202.8:c.1070T>C