Canonical Allele Identifier: PA109174
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1500944
ClinVar RCV Id: RCV002016037
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Gly386Ser
CA9135898
NM_000208.4:c.1156G>A