Allele Registry

Canonical Allele Identifier: PA108915

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015801

RCV000015802

ClinVar Variation:

14687

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Ala1161Thr	CA124225 NM_000208.4:c.3481G>A