Canonical Allele Identifier: PA2826733529
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2227029
ClinVar RCV Id: RCV002702152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Cys677Tyr
CA5903344
NM_001287174.3:c.2030G>A