Allele Registry

Canonical Allele Identifier: PA109054

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015798

ClinVar Variation:

14684

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Arg762Ser	CA124221 NM_000208.4:c.2286G>T CA403662773 NM_000208.4:c.2286G>C