Canonical Allele Identifier: PA2825802649
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3109565
ClinVar RCV Id: RCV004397911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136046.1:p.Thr247Ser
CA369168500
NM_001142574.2:c.740C>G
CA369168504
NM_001142574.2:c.739A>T