Canonical Allele Identifier: PA124378
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899066.1:p.Arg154Trp
CA124376
NM_183243.3:c.460C>T