Canonical Allele Identifier: PA2825148690
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 265022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Lys1343Met
CA10588515
NM_000352.6:c.4028A>T