Canonical Allele Identifier: PA124387
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14838
ClinVar RCV Id: RCV000015963
ClinVar Variation Id: 1457411
ClinVar RCV Id: RCV001972635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Asn250Lys
CA124382
NM_001142576.2:c.750T>G
CA369171839
NM_001142576.2:c.750T>A