Canonical Allele Identifier: PA2825548433
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866594
ClinVar RCV Id: RCV001074713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001096075.1:p.Lys303_Lys304insPhe
CA916082962
NM_001102605.2:c.909_910insTTC