Allele Registry

Canonical Allele Identifier: PA109384

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015817

ClinVar Variation:

14702

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Val55Ala	CA124253 NM_000208.4:c.164T>C