Canonical Allele Identifier: PA2830411802
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 449198
ClinVar RCV Id: RCV000522125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899066.1:p.Ala489Thr
CA4470784
NM_183243.3:c.1465G>A