Canonical Allele Identifier: PA916030810
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 157709
ClinVar RCV Id: RCV000145007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.His293Pro
CA270980
NM_001351295.2:c.878A>C