Canonical Allele Identifier: PA120109
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Arg1353His
CA120108
NM_001287174.3:c.4058G>A