Allele Registry

Canonical Allele Identifier: PA108661

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014320

RCV001089455

RCV001818156

ClinVar Variation:

13388

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Ala24Asp	CA341284 NM_000207.3:c.71C>A