Canonical Allele Identifier: PA645438464
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 303784
ClinVar RCV Id: RCV000283129 RCV000318290 RCV000375274 RCV002253382 RCV002261041 RCV002520704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Arg285Trp
CA5903741
NM_001287174.3:c.853C>T