Canonical Allele Identifier: PA658802927
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 504474
ClinVar RCV Id: RCV000599040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Ile56Thr
CA403160537
NM_000208.4:c.167T>C