Canonical Allele Identifier: PA916030915
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Arg1374His
CA120108
NM_001351295.2:c.4121G>A