Canonical Allele Identifier: PA2741812327
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2792404
ClinVar RCV Id: RCV003667208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Arg914His
CA403672105
NM_000208.4:c.2741G>A