Canonical Allele Identifier: PA2825803937
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866652
ClinVar RCV Id: RCV001074838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Asn282Lys
CA369169244
NM_001142576.2:c.846C>G
CA369169245
NM_001142576.2:c.846C>A