Canonical Allele Identifier: PA2827604906
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 265022
ClinVar RCV Id: RCV000255823 RCV001833295 RCV002244727 RCV002244726 RCV002487167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Lys1343Met
CA10588515
NM_001351296.2:c.4028A>T