Allele Registry

Canonical Allele Identifier: PA1139672508

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV001174371

ClinVar Variation:

917412

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Lys487Gln	CA403667101 NM_001079817.3:c.1459A>C