Allele Registry

Canonical Allele Identifier: PA2826155697

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020205

RCV003445081

ClinVar Variation:

21115

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172027.1:p.Gly47Val	CA341643 NM_001185098.2:c.140G>T