Canonical Allele Identifier: PA2830411571
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3109565
ClinVar RCV Id: RCV004397911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899066.1:p.Thr301Ser
CA369168500
NM_183243.3:c.902C>G
CA369168504
NM_183243.3:c.901A>T