Canonical Allele Identifier: PA916030922
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 554195
ClinVar RCV Id: RCV000669782 RCV000710385 RCV003465494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Gly1400Arg
CA379788454
NM_001351295.2:c.4198G>C