Allele Registry

Canonical Allele Identifier: PA124242

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015810

RCV001753417

ClinVar Variation:

14695

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Asn489Ser	CA124241 NM_001079817.3:c.1466A>G