Canonical Allele Identifier: PA2825803285
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3109565
ClinVar RCV Id: RCV004397911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Thr227Ser
CA369168500
NM_001142575.2:c.680C>G
CA369168504
NM_001142575.2:c.679A>T