Canonical Allele Identifier: PA2580322910
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1754276
ClinVar RCV Id: RCV002364484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006114.1:p.Phe219Leu
CA414522238
NM_006123.5:c.657C>G
CA414522239
NM_006123.5:c.657C>A
CA414522244
NM_006123.5:c.655T>C