Canonical Allele Identifier: PA1139672426
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 893023
ClinVar RCV Id: RCV001130137 RCV001130138 RCV001130139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Asp261Glu
CA9136014
NM_001079817.3:c.783C>G
CA304866609
NM_001079817.3:c.783C>A