Canonical Allele Identifier: PA2573063808
Gene: IMPDH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305966
ClinVar RCV Id: RCV001766919
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000875.2:p.Gly207Arg
CA352741476
NM_000884.3:c.619G>C
CA352741477
NM_000884.3:c.619G>A