Canonical Allele Identifier: PA1139729569
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 977713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Gln485Lys
CA379766919
NM_001351295.2:c.1453C>A