Canonical Allele Identifier: PA2741812337
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2634452
ClinVar RCV Id: RCV003732569 RCV004531714
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Glu1307Lys
CA9135120
NM_000208.4:c.3919G>A