Allele Registry

Canonical Allele Identifier: PA206381

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000193115

RCV004020319

ClinVar Variation:

211191

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Gly765Ser	CA206380 NM_000208.4:c.2293G>A