Allele Registry

Canonical Allele Identifier: PA124230

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015805

ClinVar Variation:

14690

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Phe409Val	CA124229 NM_001079817.3:c.1225T>G