Allele Registry

Canonical Allele Identifier: PA2741812335

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV004536708

ClinVar Variation:

2637065

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Ala1162Val	CA403670207 NM_000208.4:c.3485C>T