Canonical Allele Identifier: PA2826733791
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1729810
ClinVar RCV Id: RCV002326137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.His1098Tyr
CA379801445
NM_001287174.3:c.3292C>T