Canonical Allele Identifier: PA2825397158
Gene: INS-IGF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035835.1:p.Arg55Cys
CA123087
NM_001042376.3:c.163C>T