Canonical Allele Identifier: PA206065
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 210076
ClinVar RCV Id: RCV000192916 RCV001640282 RCV002051825 RCV002500586 RCV002517038 RCV003987437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Arg1182Trp
CA206064
NM_000352.6:c.3544C>T