Canonical Allele Identifier: PA2827603904
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 371380
ClinVar RCV Id: RCV000409175 RCV001203709 RCV002230219 RCV001828376 RCV002502430 RCV003463804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Arg74Trp
CA5903947
NM_001351296.2:c.220C>T