Canonical Allele Identifier: PA2825803232
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866754
ClinVar RCV Id: RCV001075040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Arg206Gln
CA369169226
NM_001142575.2:c.617G>A