Allele Registry

Canonical Allele Identifier: PA109346

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015797

ClinVar Variation:

14683

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Trp1227Ser	CA124220 NM_000208.4:c.3680G>C