Canonical Allele Identifier: PA2580109748
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2414166
ClinVar RCV Id: RCV003106499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Arg1053Cys
CA9135350
NM_000208.4:c.3157C>T