Canonical Allele Identifier: PA2827604980
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2678780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Met1394Arg
CA379787876
NM_001351296.2:c.4181T>G