Allele Registry

Canonical Allele Identifier: PA916018263

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020205

RCV003445081

ClinVar Variation:

21115

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278826.1:p.Gly47Val	CA341643 NM_001291897.2:c.140G>T