Canonical Allele Identifier: PA2825147721
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_000343.2:p.Arg275Trp
CA5903743
NM_000352.6:c.823C>T