Canonical Allele Identifier: PA2826894676
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 194714
ClinVar RCV Id: RCV000175148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Arg528Trp
CA240847
NM_001304521.2:c.1582C>T