Canonical Allele Identifier: PA2573071051
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1311162
ClinVar RCV Id: RCV001758671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Ile1425Thr
CA379787397
NM_001351295.2:c.4274T>C