Canonical Allele Identifier: PA2825447913
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 330455
ClinVar RCV Id: RCV000267106 RCV000320530 RCV000380386 RCV001820999 RCV002521258 RCV002504115 RCV002521259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Thr846Met
CA9135511
NM_001079817.3:c.2537C>T