Canonical Allele Identifier: PA2741829857
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2884081
ClinVar RCV Id: RCV003724240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Gln695Arg
CA9135670
NM_001079817.3:c.2084A>G