Allele Registry

Canonical Allele Identifier: PA2825397107

Gene: INS-IGF2 HGNC NCBI

ClinVar RCV:

RCV000020213

ClinVar Variation:

21123

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035835.1:p.Gly32Arg	CA341647 NM_001042376.3:c.94G>C