Canonical Allele Identifier: PA097615
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 18449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Gly716Val
CA220124
NM_000352.6:c.2147G>T