Canonical Allele Identifier: PA2827605969
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2576202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Leu1146Arg
CA379798436
NM_001351297.2:c.3437T>G