Allele Registry

Canonical Allele Identifier: PA108683

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014324

RCV001558886

RCV003445069

RCV003987320

ClinVar Variation:

13392

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Arg55Cys	CA123087 NM_000207.3:c.163C>T