Canonical Allele Identifier: PA207379
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 210068
ClinVar RCV Id: RCV000193705 RCV000303097 RCV000396751 RCV000360233 RCV001279195 RCV001336811 RCV001546216 RCV002514096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Ile462Val
CA207378
NM_000352.6:c.1384A>G