Allele Registry

Canonical Allele Identifier: PA2825801948

Gene: IMPDH1 HGNC NCBI

ClinVar RCV:

RCV000415244

RCV001198950

ClinVar Variation:

374177

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136045.1:p.Thr225Pro	CA16043423 NM_001142573.2:c.673A>C