Canonical Allele Identifier: PA120113
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Arg1380Cys
CA120112
NM_001287174.3:c.4138C>T