Allele Registry

Canonical Allele Identifier: PA209133

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000194753

RCV003580793

ClinVar Variation:

211199

2770673

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.His28Gln	CA209132 NM_000208.4:c.84C>A CA403162512 NM_000208.4:c.84C>G