Allele Registry

Canonical Allele Identifier: PA2825084723

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV001174371

ClinVar Variation:

917412

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Lys487Gln	CA403667101 NM_000208.4:c.1459A>C