Allele Registry

Canonical Allele Identifier: PA109200

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015808

ClinVar Variation:

14693

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.His236Arg	CA124236 NM_000208.4:c.707A>G