Canonical Allele Identifier: PA108942
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14697
ClinVar RCV Id: RCV000015812 RCV002496377
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Arg1020Gln
CA124245
NM_000208.4:c.3059G>A