Canonical Allele Identifier: PA2826894508
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 931699
ClinVar RCV Id: RCV001198547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Lys254Thr
CA369169020
NM_001304521.2:c.761A>C