Canonical Allele Identifier: PA2827605116
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 434043
ClinVar RCV Id: RCV000500617 RCV000514132 RCV001174390 RCV002244966 RCV002244967
ClinVar Variation Id: 554959
ClinVar RCV Id: RCV000670686
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Lys1521Asn
CA5902427
NM_001351296.2:c.4563G>T
CA379782126
NM_001351296.2:c.4563G>C