Canonical Allele Identifier: PA257391
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001096075.1:p.Arg299Pro
CA257385
NM_001102605.2:c.896G>C