Canonical Allele Identifier: PA916030834
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 210069
ClinVar RCV Id: RCV000194750 RCV002514097 RCV003387795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Leu511Pro
CA277373
NM_001351295.2:c.1532T>C