Canonical Allele Identifier: PA1139682304
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_000199.2:p.Val866Ile
CA9135504
NM_000208.4:c.2596G>A