Canonical Allele Identifier: PA2573164544
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1486096
ClinVar RCV Id: RCV002001226
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Glu1313Lys
CA9135116
NM_000208.4:c.3937G>A