Allele Registry

Canonical Allele Identifier: PA109093

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015810

RCV001753417

ClinVar Variation:

14695

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Asn489Ser	CA124241 NM_000208.4:c.1466A>G