Canonical Allele Identifier: PA2580193259
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2164615
ClinVar RCV Id: RCV003088124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Met86Val
CA4471151
NM_001304521.2:c.256A>G