Canonical Allele Identifier: PA2825803252
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715850
ClinVar RCV Id: RCV002301560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Ser215Phe
CA369168879
NM_001142575.2:c.644C>T