Canonical Allele Identifier: PA2825084934
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 3109938
ClinVar RCV Id: RCV004398284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.His1295Gln
CA403668778
NM_000208.4:c.3885C>G
CA403668779
NM_000208.4:c.3885C>A