Allele Registry

Canonical Allele Identifier: PA108714

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020207

RCV001089453

RCV002051790

RCV002513137

ClinVar Variation:

21117

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Arg89Cys	CA341644 NM_000207.3:c.265C>T