Canonical Allele Identifier: PA2827603030
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Pro45Leu
CA254640
NM_001351295.2:c.134C>T