Canonical Allele Identifier: PA2825801972
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371890
ClinVar RCV Id: RCV001879212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136045.1:p.Lys238Asn
CA369168984
NM_001142573.2:c.714G>T
CA369168990
NM_001142573.2:c.714G>C