Allele Registry

Canonical Allele Identifier: PA2826155658

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020210

RCV003389036

ClinVar Variation:

21120

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172026.1:p.Tyr108Cys	CA341646 NM_001185097.2:c.323A>G