Canonical Allele Identifier: PA108961
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14703
ClinVar RCV Id: RCV000015818
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Arg113Pro
CA124255
NM_000208.4:c.338G>C