Canonical Allele Identifier: PA2827606231
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 434057
ClinVar RCV Id: RCV000501443 RCV002244972 RCV002244971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Ser1421Cys
CA379786606
NM_001351297.2:c.4262C>G