Canonical Allele Identifier: PA124246
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14697
ClinVar RCV Id: RCV000015812 RCV002496377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Arg1008Gln
CA124245
NM_001079817.3:c.3023G>A