Canonical Allele Identifier: PA257388
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14836
ClinVar RCV Id: RCV000015961 RCV003887872
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136045.1:p.Arg224Pro
CA257385
NM_001142573.2:c.671G>C