Allele Registry

Canonical Allele Identifier: PA109361

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015825

ClinVar Variation:

14710

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Trp439Ser	CA124269 NM_000208.4:c.1316G>C