Canonical Allele Identifier: PA2825448139
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2634452
ClinVar RCV Id: RCV003732569 RCV004531714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Glu1295Lys
CA9135120
NM_001079817.3:c.3883G>A