Canonical Allele Identifier: PA2825803241
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 812335
ClinVar RCV Id: RCV001003054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Leu210Pro
CA369169111
NM_001142575.2:c.629T>C