Canonical Allele Identifier: PA205177
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 210067
ClinVar RCV Id: RCV000192390 RCV000666629 RCV000763720 RCV000710372 RCV001272242 RCV001336810 RCV001102903 RCV001102904 RCV001449652 RCV003491936 RCV004530090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Cys418Arg
CA205176
NM_001287174.3:c.1252T>C