Canonical Allele Identifier: PA2499234397
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_000874.2:p.Ala351Glu
CA369167963
NM_000883.4:c.1052C>A