Canonical Allele Identifier: PA658832652
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_001274103.1:p.Ala1367Thr
CA379790329
NM_001287174.3:c.4099G>A