Canonical Allele Identifier: PA2827604089
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1807338
ClinVar RCV Id: RCV002475295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Arg274Trp
CA5903743
NM_001351296.2:c.820C>T