Canonical Allele Identifier: PA2825801973
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 937932
ClinVar RCV Id: RCV001207064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136045.1:p.Lys238Arg
CA369169029
NM_001142573.2:c.713A>G