Canonical Allele Identifier: PA2825447979
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 211195
ClinVar RCV Id: RCV000194649 RCV000286740 RCV000341695 RCV000445398 RCV000382385 RCV000725784 RCV004530121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Asp934Glu
CA208959
NM_001079817.3:c.2802C>G
CA403671905
NM_001079817.3:c.2802C>A