Canonical Allele Identifier: PA2826894497
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866652
ClinVar RCV Id: RCV001074838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Asn246Lys
CA369169244
NM_001304521.2:c.738C>G
CA369169245
NM_001304521.2:c.738C>A