Canonical Allele Identifier: PA109246
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14689
ClinVar RCV Id: RCV000015804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Leu260Pro
CA124227
NM_000208.4:c.779T>C