Canonical Allele Identifier: PA2827606202
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_001338226.1:p.Met1393Val
CA218408197
NM_001351297.2:c.4177A>G