Canonical Allele Identifier: PA2827604968
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 446775
ClinVar RCV Id: RCV000517310 RCV003313963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Ser1386Phe
CA218408231
NM_001351296.2:c.4157C>T