Canonical Allele Identifier: PA658832663
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 556519
ClinVar RCV Id: RCV000672538 RCV000710392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Ala1537Val
CA5902421
NM_001287174.3:c.4610C>T