Allele Registry

Canonical Allele Identifier: PA2825448087

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV004536708

ClinVar Variation:

2637065

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Ala1150Val	CA403670207 NM_001079817.3:c.3449C>T