Canonical Allele Identifier: PA109158
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14679
ClinVar RCV Id: RCV000015793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Gly1035Val
CA124211
NM_000208.4:c.3104G>T