Allele Registry

Canonical Allele Identifier: PA2826155692

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020204

RCV000030069

RCV001089452

RCV003445080

ClinVar Variation:

21114

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172027.1:p.Cys43Gly	CA214063 NM_001185098.2:c.127T>G