Canonical Allele Identifier: PA2825803248
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 937932
ClinVar RCV Id: RCV001207064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Lys213Arg
CA369169029
NM_001142575.2:c.638A>G