Allele Registry

Canonical Allele Identifier: PA2826155730

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014319

RCV000517445

RCV001089454

RCV002051784

ClinVar Variation:

13387

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172027.1:p.Cys96Tyr	CA341283 NM_001185098.2:c.287G>A