Allele Registry

Canonical Allele Identifier: PA109268

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015794

ClinVar Variation:

14680

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Lys487Glu	CA124213 NM_000208.4:c.1459A>G