Allele Registry

Canonical Allele Identifier: PA124246

Gene: INSR HGNC NCBI

ClinVar Allele:

29736

ClinVar RCV:

RCV000015812

RCV002496377

ClinVar Variation:

14697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Arg1008Gln	CA124245 NM_001079817.3:c.3023G>A