Canonical Allele Identifier: PA2827604901
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 557922
ClinVar RCV Id: RCV000674122 RCV002245577 RCV002245576
ClinVar Variation Id: 1476628
ClinVar RCV Id: RCV002014869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Trp1338Arg
CA379791109
NM_001351296.2:c.4012T>C
CA379791113
NM_001351296.2:c.4012T>A