Canonical Allele Identifier: PA124214
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14680
ClinVar RCV Id: RCV000015794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Lys487Glu
CA124213
NM_001079817.3:c.1459A>G