Allele Registry

Canonical Allele Identifier: PA108993

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015815

ClinVar Variation:

14700

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Arg1191Gln	CA124248 NM_000208.4:c.3572G>A