Allele Registry

Canonical Allele Identifier: PA2826155729

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000059612

ClinVar Variation:

68730

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172027.1:p.Cys96Ser	CA266173 NM_001185098.2:c.287G>C CA379120862 NM_001185098.2:c.286T>A