Canonical Allele Identifier: PA200289
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 193063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Ala2Gly
CA200288
NM_000208.4:c.5C>G