Canonical Allele Identifier: PA2825084625
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 893023
ClinVar RCV Id: RCV001130137 RCV001130138 RCV001130139
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Asp261Glu
CA9136014
NM_000208.4:c.783C>G
CA304866609
NM_000208.4:c.783C>A