Canonical Allele Identifier: PA2827602994
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 495835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Val21Asp
CA5903992
NM_001351295.2:c.62T>A