Canonical Allele Identifier: PA2827604923
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2576198
ClinVar RCV Id: RCV003322259 RCV003561296 RCV003466059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Pro1359Leu
CA5902590
NM_001351296.2:c.4076C>T