Allele Registry

Canonical Allele Identifier: PA2826155602

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020213

ClinVar Variation:

21123

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172026.1:p.Gly32Arg	CA341647 NM_001185097.2:c.94G>C