Allele Registry

Canonical Allele Identifier: PA108771

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014319

RCV000517445

RCV001089454

RCV002051784

ClinVar Variation:

13387

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Cys96Tyr	CA341283 NM_000207.3:c.287G>A