Canonical Allele Identifier: PA645509690
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 439840
ClinVar RCV Id: RCV000506622
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Gly1223Asp
CA403669284
NM_000208.4:c.3668G>A