Canonical Allele Identifier: PA2826734001
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1520966
ClinVar RCV Id: RCV002031025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Met1395Val
CA218408197
NM_001287174.3:c.4183A>G