Allele Registry

Canonical Allele Identifier: PA108670

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014323

RCV001851851

RCV003445068

ClinVar Variation:

13391

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Arg46Gln	CA123086 NM_000207.3:c.137G>A