Canonical Allele Identifier: PA2825803955
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 937932
ClinVar RCV Id: RCV001207064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Lys290Arg
CA369169029
NM_001142576.2:c.869A>G