Allele Registry

Canonical Allele Identifier: PA2826155718

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014313

ClinVar Variation:

13382

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172027.1:p.Arg89Leu	CA123082 NM_001185098.2:c.266G>T