Allele Registry

Canonical Allele Identifier: PA124222

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015798

ClinVar Variation:

14684

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Arg750Ser	CA124221 NM_001079817.3:c.2250G>T CA403662773 NM_001079817.3:c.2250G>C