Canonical Allele Identifier: PA257387
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_001136046.1:p.Arg219Pro
CA257385
NM_001142574.2:c.656G>C