Allele Registry

Canonical Allele Identifier: PA2826155678

Gene: INS HGNC NCBI

ClinVar RCV:

RCV000030071

RCV001818190

ClinVar Variation:

36401

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172027.1:p.Ala24Val	CA214065 NM_001185098.2:c.71C>T