Allele Registry

Canonical Allele Identifier: PA124258

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015819

ClinVar Variation:

14704

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Ala1150Glu	CA124257 NM_001079817.3:c.3449C>A