Canonical Allele Identifier: PA2830411541
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 931699
ClinVar RCV Id: RCV001198547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899066.1:p.Lys287Thr
CA369169020
NM_183243.3:c.860A>C