Canonical Allele Identifier: PA2826894517
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3109565
ClinVar RCV Id: RCV004397911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Thr268Ser
CA369168500
NM_001304521.2:c.803C>G
CA369168504
NM_001304521.2:c.802A>T