Canonical Allele Identifier: PA2825802602
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866652
ClinVar RCV Id: RCV001074838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136046.1:p.Asn225Lys
CA369169244
NM_001142574.2:c.675C>G
CA369169245
NM_001142574.2:c.675C>A