Canonical Allele Identifier: PA2826734123
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2884032
ClinVar RCV Id: RCV003724222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Ala1537Thr
CA5902422
NM_001287174.3:c.4609G>A