Canonical Allele Identifier: PA097988
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 804491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Thr1138Met
CA5902811
NM_000352.6:c.3413C>T