Canonical Allele Identifier: PA2825148694
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 549539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Asn1348Ser
CA379790767
NM_000352.6:c.4043A>G