Canonical Allele Identifier: PA2825148528
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2307381
ClinVar RCV Id: RCV002879623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Leu1164Phe
CA379797987
NM_000352.6:c.3490C>T