Allele Registry

Canonical Allele Identifier: PA2825447874

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000193115

RCV004020319

ClinVar Variation:

211191

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Gly753Ser	CA206380 NM_001079817.3:c.2257G>A