Canonical Allele Identifier: PA2830411480
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1380019
ClinVar RCV Id: RCV001917109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899066.1:p.Asp265Gly
CA369169685
NM_183243.3:c.794A>G