Allele Registry

Canonical Allele Identifier: PA915964979

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015814

ClinVar Variation:

14699

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Gly58Arg	CA124247 NM_001079817.3:c.172G>A CA403160518 NM_001079817.3:c.172G>C