Allele Registry

Canonical Allele Identifier: PA2826155717

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014315

ClinVar Variation:

13383

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172027.1:p.Arg89Pro	CA123083 NM_001185098.2:c.266G>C