Allele Registry

Canonical Allele Identifier: PA2826155635

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020207

RCV001089453

RCV002051790

RCV002513137

ClinVar Variation:

21117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172026.1:p.Arg89Cys	CA341644 NM_001185097.2:c.265C>T