Allele Registry

Canonical Allele Identifier: PA124237

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015808

ClinVar Variation:

14693

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.His236Arg	CA124236 NM_001079817.3:c.707A>G