Allele Registry

Canonical Allele Identifier: PA108695

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014322

ClinVar Variation:

13390

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Arg6Cys	CA123085 NM_000207.3:c.16C>T