Allele Registry

Canonical Allele Identifier: PA645490551

Gene: IMPG2 HGNC NCBI

ClinVar Variation Id: 342339

HGVS (amino-acid)	Matching Registered Transcripts
NP_057331.2:p.Arg1048Trp	CA2518823 NM_016247.4:c.3142C>T