Canonical Allele Identifier: PA913193001
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 593002
ClinVar RCV Id: RCV000727925
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Asn1288Ser
CA9135128
NM_000208.4:c.3863A>G