Allele Registry

Canonical Allele Identifier: PA915964974

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_001073285.1:p.Leu14Pro	CA9136191 NM_001079817.3:c.41T>C