Allele Registry

Canonical Allele Identifier: PA124232

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015806

ClinVar Variation:

14691

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Asn42Lys	CA124231 NM_001079817.3:c.126C>A CA403160696 NM_001079817.3:c.126C>G