Canonical Allele Identifier: PA915964977
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_001073285.1:p.Ile56Thr
CA403160537
NM_001079817.3:c.167T>C