Allele Registry

Canonical Allele Identifier: PA109285

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015805

ClinVar Variation:

14690

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Phe409Val	CA124229 NM_000208.4:c.1225T>G