Allele Registry

Canonical Allele Identifier: PA2825211501

Gene: IMPDH1 HGNC NCBI

ClinVar Variation Id: 910851

HGVS (amino-acid)	Matching Registered Transcripts
NP_000874.2:p.Arg142Trp	CA4471164 NM_000883.4:c.424C>T