Allele Registry

Canonical Allele Identifier: PA108806

Gene: INS HGNC NCBI

ClinVar Allele:

33970

ClinVar RCV:

RCV000020208

RCV003460486

ClinVar Variation:

21118

HGVS (amino-acid)	Matching Registered Transcripts
NP_000198.1:p.Gly90Cys	CA341645 NM_000207.3:c.268G>T