Canonical Allele Identifier: PA2826733818
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2576202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Leu1148Arg
CA379798436
NM_001287174.3:c.3443T>G