Canonical Allele Identifier: PA2825447922
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 892864
ClinVar RCV Id: RCV001129682 RCV001129680 RCV001129681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Val854Ile
CA9135504
NM_001079817.3:c.2560G>A