Canonical Allele Identifier: PA2825548439
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866754
ClinVar RCV Id: RCV001075040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001096075.1:p.Arg306Gln
CA369169226
NM_001102605.2:c.917G>A