Canonical Allele Identifier: PA2827604758
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1210344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Val1155Ile
CA5902800
NM_001351296.2:c.3463G>A