Canonical Allele Identifier: PA2825448168
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 330439
ClinVar RCV Id: RCV000287779 RCV000328762 RCV000383396
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Arg1331Gln
CA9135101
NM_001079817.3:c.3992G>A