Canonical Allele Identifier: PA2827603917
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9111
ClinVar RCV Id: RCV000009681 RCV001089462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Val86Gly
CA340877
NM_001351296.2:c.257T>G