Canonical Allele Identifier: PA2825802018
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026578
ClinVar RCV Id: RCV001327046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136045.1:p.Ala266Glu
CA369167963
NM_001142573.2:c.797C>A