Canonical Allele Identifier: PA915964972
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 193063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Ala2Gly
CA200288
NM_001079817.3:c.5C>G