Canonical Allele Identifier: PA2826894491
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2735088
ClinVar RCV Id: RCV003555371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Leu243Pro
CA369169375
NM_001304521.2:c.728T>C