Canonical Allele Identifier: PA2580216149
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2137006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Ile1533Thr
CA379782757
NM_001351295.2:c.4598T>C