Allele Registry

Canonical Allele Identifier: PA124249

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015815

ClinVar Variation:

14700

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Arg1179Gln	CA124248 NM_001079817.3:c.3536G>A