Canonical Allele Identifier: PA2827605067
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 434045
ClinVar RCV Id: RCV000503504 RCV000763232 RCV000710389 RCV003470623 RCV001848864 RCV003330733
ClinVar Variation Id: 3233553
ClinVar RCV Id: RCV004526403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Gly1478Arg
CA218406864
NM_001351296.2:c.4432G>A
CA379783645
NM_001351296.2:c.4432G>C