Canonical Allele Identifier: PA2827605115
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_001338225.1:p.Leu1519Phe
CA379782201
NM_001351296.2:c.4555C>T