Canonical Allele Identifier: PA2580215996
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2227029
ClinVar RCV Id: RCV002702152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Cys699Tyr
CA5903344
NM_001351295.2:c.2096G>A