Canonical Allele Identifier: PA658826997
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 549553
ClinVar RCV Id: RCV000664157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Arg581Trp
CA403666437
NM_000208.4:c.1741C>T