Canonical Allele Identifier: PA2825448196
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1685300
ClinVar RCV Id: RCV002249027 RCV003094009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Arg1366Gln
CA9135084
NM_001079817.3:c.4097G>A