Canonical Allele Identifier: PA2825084617
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2277295
ClinVar RCV Id: RCV002813616 RCV003491279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Asp247Asn
CA9136022
NM_000208.4:c.739G>A