Canonical Allele Identifier: PA2830411298
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2796009
ClinVar RCV Id: RCV003667930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899066.1:p.Met119Ile
CA369174447
NM_183243.3:c.357G>T
CA369174449
NM_183243.3:c.357G>C
CA369174451
NM_183243.3:c.357G>A