Allele Registry

Canonical Allele Identifier: PA916018271

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020207

RCV001089453

RCV002051790

RCV002513137

ClinVar Variation:

21117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278826.1:p.Arg89Cys	CA341644 NM_001291897.2:c.265C>T