Canonical Allele Identifier: PA645402359
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 435518
ClinVar RCV Id: RCV000500908 RCV001129887 RCV001129888 RCV001129889 RCV002527259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Ala706Asp
CA9135660
NM_000208.4:c.2117C>A