Allele Registry

Canonical Allele Identifier: PA108791

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020212

RCV000030072

RCV000117279

RCV001089451

RCV001775542

ClinVar Variation:

21122

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Gly32Ser	CA214067 NM_000207.3:c.94G>A