Canonical Allele Identifier: PA916030919
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 557361
ClinVar RCV Id: RCV000673493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Ala1388Thr
CA379790329
NM_001351295.2:c.4162G>A