Canonical Allele Identifier: PA916030926
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Arg1401Cys
CA120112
NM_001351295.2:c.4201C>T