Canonical Allele Identifier: PA2580109761
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2012772
ClinVar RCV Id: RCV002843358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Arg1163Ser
CA403670195
NM_000208.4:c.3489A>T
CA403670196
NM_000208.4:c.3489A>C