Canonical Allele Identifier: PA2825801958
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866656
ClinVar RCV Id: RCV001074851
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136045.1:p.Asn230Tyr
CA369169260
NM_001142573.2:c.688A>T