Canonical Allele Identifier: PA2825803194
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1380019
ClinVar RCV Id: RCV001917109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Asp191Gly
CA369169685
NM_001142575.2:c.572A>G