Allele Registry

Canonical Allele Identifier: PA108961

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015818

ClinVar Variation:

14703

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Arg113Pro	CA124255 NM_000208.4:c.338G>C