Canonical Allele Identifier: PA2826733187
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 878389
ClinVar RCV Id: RCV001104909 RCV001104910 RCV001104908 RCV002253776 RCV002253775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Ile196Asn
CA379779450
NM_001287174.3:c.587T>A