Allele Registry

Canonical Allele Identifier: PA124214

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015794

ClinVar Variation:

14680

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Lys487Glu	CA124213 NM_001079817.3:c.1459A>G