Allele Registry

Canonical Allele Identifier: PA916018283

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020210

RCV003389036

ClinVar Variation:

21120

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278826.1:p.Tyr108Cys	CA341646 NM_001291897.2:c.323A>G