Allele Registry

Canonical Allele Identifier: PA124216

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015795

ClinVar Variation:

14681

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Gly393Arg	CA124215 NM_001079817.3:c.1177G>A CA403667742 NM_001079817.3:c.1177G>C