Canonical Allele Identifier: PA1139690542
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 910851
ClinVar RCV Id: RCV001162958 RCV001162959 RCV002558560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Arg73Trp
CA4471164
NM_001304521.2:c.217C>T