Allele Registry

Canonical Allele Identifier: PA109246

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015804

ClinVar Variation:

14689

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Leu260Pro	CA124227 NM_000208.4:c.779T>C