Allele Registry

Canonical Allele Identifier: PA2826155667

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000014322

ClinVar Variation:

13390

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172027.1:p.Arg6Cys	CA123085 NM_001185098.2:c.16C>T