Allele Registry

Canonical Allele Identifier: PA2825084612

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV001358257

ClinVar Variation:

1050616

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Leu233Arg	CA403670567 NM_000208.4:c.698T>G