Allele Registry

Canonical Allele Identifier: PA109083

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015829

ClinVar Variation:

14714

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Asn458Asp	CA124275 NM_000208.4:c.1372A>G