Canonical Allele Identifier: PA2826894407
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14837
ClinVar RCV Id: RCV000015962 RCV000951177 RCV003887873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Arg121Trp
CA124376
NM_001304521.2:c.361C>T