Allele Registry

Canonical Allele Identifier: PA109074

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015806

ClinVar Variation:

14691

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Asn42Lys	CA124231 NM_000208.4:c.126C>A CA403160696 NM_000208.4:c.126C>G