Allele Registry

Canonical Allele Identifier: PA915964975

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000194753

RCV003580793

ClinVar Variation:

211199

2770673

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.His28Gln	CA209132 NM_001079817.3:c.84C>A CA403162512 NM_001079817.3:c.84C>G