Canonical Allele Identifier: PA2825148798
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1464709
ClinVar RCV Id: RCV001956958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Arg1420Ser
CA379786677
NM_000352.6:c.4258C>A