Canonical Allele Identifier: PA2827604920
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1339207
ClinVar RCV Id: RCV001823661 RCV004536349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Asp1354Asn
CA379790603
NM_001351296.2:c.4060G>A