Canonical Allele Identifier: PA2825801794
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2181397
ClinVar RCV Id: RCV002595629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136045.1:p.Ala76Val
CA369174375
NM_001142573.2:c.227C>T