Canonical Allele Identifier: PA2826894631
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_001291450.1:p.Ala456Thr
CA4470784
NM_001304521.2:c.1366G>A