Allele Registry

Canonical Allele Identifier: PA2826155707

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014324

RCV001558886

RCV003445069

RCV003987320

ClinVar Variation:

13392

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172027.1:p.Arg55Cys	CA123087 NM_001185098.2:c.163C>T