Allele Registry

Canonical Allele Identifier: PA108729

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014310

RCV001091846

RCV003407328

ClinVar Variation:

13380

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Arg89His	CA123079 NM_000207.3:c.266G>A