Allele Registry

Canonical Allele Identifier: PA916018262

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014323

RCV001851851

RCV003445068

ClinVar Variation:

13391

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278826.1:p.Arg46Gln	CA123086 NM_001291897.2:c.137G>A