Canonical Allele Identifier: PA2741812331
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2858657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Arg1068Gln
CA9135335
NM_000208.4:c.3203G>A