Canonical Allele Identifier: PA257386
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Arg199Pro
CA257385
NM_001142575.2:c.596G>C