Canonical Allele Identifier: PA2827604718
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1729810
ClinVar RCV Id: RCV002326137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.His1097Tyr
CA379801445
NM_001351296.2:c.3289C>T