Canonical Allele Identifier: PA2825803611
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 194714
ClinVar RCV Id: RCV000175148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Arg487Trp
CA240847
NM_001142575.2:c.1459C>T