Canonical Allele Identifier: PA2825803522
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 449198
ClinVar RCV Id: RCV000522125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Ala415Thr
CA4470784
NM_001142575.2:c.1243G>A