Canonical Allele Identifier: PA2827604891
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 288731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Glu1326Lys
CA5902631
NM_001351296.2:c.3976G>A