Canonical Allele Identifier: PA2827604451
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 18449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Gly715Val
CA220124
NM_001351296.2:c.2144G>T