Canonical Allele Identifier: PA645438541
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 303766
ClinVar RCV Id: RCV000292832 RCV000352427 RCV000394844 RCV001278400 RCV002250621 RCV002251452 RCV002056180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Asp1039Asn
CA5902919
NM_001287174.3:c.3115G>A