Allele Registry

Canonical Allele Identifier: PA2825448110

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015797

ClinVar Variation:

14683

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Trp1215Ser	CA124220 NM_001079817.3:c.3644G>C