Canonical Allele Identifier: PA645402489
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 330439
ClinVar RCV Id: RCV000287779 RCV000328762 RCV000383396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Arg1343Gln
CA9135101
NM_000208.4:c.4028G>A