Allele Registry

Canonical Allele Identifier: PA108781

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020213

ClinVar Variation:

21123

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Gly32Arg	CA341647 NM_000207.3:c.94G>C