Canonical Allele Identifier: PA2825803238
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1513705
ClinVar RCV Id: RCV002026303 RCV003303647
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Tyr208His
CA369169194
NM_001142575.2:c.622T>C