Allele Registry

Canonical Allele Identifier: PA108799

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020205

RCV003445081

ClinVar Variation:

21115

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Gly47Val	CA341643 NM_000207.3:c.140G>T