Canonical Allele Identifier: PA2825448133
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 3109938
ClinVar RCV Id: RCV004398284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.His1283Gln
CA403668778
NM_001079817.3:c.3849C>G
CA403668779
NM_001079817.3:c.3849C>A