Canonical Allele Identifier: PA2825447933
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 282255
ClinVar RCV Id: RCV000361037 RCV000765478 RCV004535276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Arg877Trp
CA9135496
NM_001079817.3:c.2629C>T