Canonical Allele Identifier: PA2825212087
Gene: IMPDH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2398827
ClinVar RCV Id: RCV004231537
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000875.2:p.Lys205Arg
CA2390655
NM_000884.3:c.614A>G