Allele Registry

Canonical Allele Identifier: PA916018274

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020208

RCV003460486

ClinVar Variation:

21118

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278826.1:p.Gly90Cys	CA341645 NM_001291897.2:c.268G>T