Canonical Allele Identifier: PA2825548451
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 636176
ClinVar RCV Id: RCV000787841

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001096075.1:p.Gln316His
CA369168836
NM_001102605.2:c.948G>T
CA369168838
NM_001102605.2:c.948G>C