Canonical Allele Identifier: PA2580109775
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2231216
ClinVar RCV Id: RCV002707940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Pro1296Ser
CA403668775
NM_000208.4:c.3886C>T