Canonical Allele Identifier: PA658665459
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 446769
ClinVar RCV Id: RCV000517936 RCV002244986 RCV002274051 RCV003736800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Ala1153Val
CA379798305
NM_001287174.3:c.3458C>T