Canonical Allele Identifier: PA2826894498
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866656
ClinVar RCV Id: RCV001074851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Asn246Tyr
CA369169260
NM_001304521.2:c.736A>T