Canonical Allele Identifier: PA2825803210
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2735088
ClinVar RCV Id: RCV003555371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Leu202Pro
CA369169375
NM_001142575.2:c.605T>C