Canonical Allele Identifier: PA658665489
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 446778
ClinVar RCV Id: RCV000516737 RCV000853271 RCV001829462 RCV002244992 RCV002244991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Thr1532Pro
CA218406302
NM_001287174.3:c.4594A>C