Canonical Allele Identifier: PA2830411528
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1513705
ClinVar RCV Id: RCV002026303 RCV003303647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899066.1:p.Tyr282His
CA369169194
NM_183243.3:c.844T>C