Allele Registry

Canonical Allele Identifier: PA108999

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015823

RCV000125461

RCV001818162

ClinVar Variation:

14708

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Arg1201Gln	CA124264 NM_000208.4:c.3602G>A