Allele Registry

Canonical Allele Identifier: PA916018255

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020213

ClinVar Variation:

21123

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278826.1:p.Gly32Arg	CA341647 NM_001291897.2:c.94G>C