Allele Registry

Canonical Allele Identifier: PA108925

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015819

ClinVar Variation:

14704

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Ala1162Glu	CA124257 NM_000208.4:c.3485C>A