Allele Registry

Canonical Allele Identifier: PA108883

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000020210

RCV003389036

ClinVar Variation:

21120

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Tyr108Cys	CA341646 NM_000207.3:c.323A>G