Canonical Allele Identifier: PA2826733816
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 804491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Thr1139Met
CA5902811
NM_001287174.3:c.3416C>T