Allele Registry

Canonical Allele Identifier: PA645402324

Gene: INSR HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

273448

ClinVar RCV:

RCV000308234

RCV000365243

RCV000408260

RCV000664158

RCV000726299

RCV002518075

RCV003884445

ClinVar Variation:

289211

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Leu14Pro	CA9136191 NM_000208.4:c.41T>C