Canonical Allele Identifier: PA341687
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 21165
ClinVar RCV Id: RCV000020285 RCV003137539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Val86Ala
CA341686
NM_001287174.3:c.257T>C