Canonical Allele Identifier: PA2825148722
Gene: ABCC8 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Ala1369Thr
CA5902584
NM_000352.6:c.4105G>A