Allele Registry

Canonical Allele Identifier: PA124226

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015801

RCV000015802

ClinVar Variation:

14687

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Ala1149Thr	CA124225 NM_001079817.3:c.3445G>A