Canonical Allele Identifier: PA2826734112
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1312141
ClinVar RCV Id: RCV001761362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Leu1520Phe
CA379782201
NM_001287174.3:c.4558C>T