Canonical Allele Identifier: PA2827604937
Gene: ABCC8 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Ala1369Thr
CA5902584
NM_001351296.2:c.4105G>A