Canonical Allele Identifier: PA2826894485
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14836
ClinVar RCV Id: RCV000015961 RCV003887872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Arg240Pro
CA257385
NM_001304521.2:c.719G>C