Canonical Allele Identifier: PA658694234
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 495835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Val21Asp
CA5903992
NM_001287174.3:c.62T>A