Canonical Allele Identifier: PA2826894506
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371890
ClinVar RCV Id: RCV001879212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Lys254Asn
CA369168984
NM_001304521.2:c.762G>T
CA369168990
NM_001304521.2:c.762G>C