Canonical Allele Identifier: PA645438572
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 288731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Glu1327Lys
CA5902631
NM_001287174.3:c.3979G>A