Canonical Allele Identifier: PA2825802598
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1172714
ClinVar RCV Id: RCV001526722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136046.1:p.Lys224Glu
CA166126091
NM_001142574.2:c.670A>G