Allele Registry

Canonical Allele Identifier: PA916018270

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014310

RCV001091846

RCV003407328

ClinVar Variation:

13380

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278826.1:p.Arg89His	CA123079 NM_001291897.2:c.266G>A