Canonical Allele Identifier: PA2825148684
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 557922
ClinVar Variation Id: 1476628
ClinVar RCV Id: RCV002014869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Trp1338Arg
CA379791109
NM_000352.6:c.4012T>C
CA379791113
NM_000352.6:c.4012T>A