Canonical Allele Identifier: PA2825803249
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 931699
ClinVar RCV Id: RCV001198547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Lys213Thr
CA369169020
NM_001142575.2:c.638A>C