Canonical Allele Identifier: PA645402490
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 330438
ClinVar RCV Id: RCV000268051 RCV000323071 RCV000382182 RCV003556347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Tyr1361Cys
CA9135093
NM_000208.4:c.4082A>G