Canonical Allele Identifier: PA2830411301
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2181397
ClinVar RCV Id: RCV002595629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899066.1:p.Ala125Val
CA369174375
NM_183243.3:c.374C>T