Canonical Allele Identifier: PA2827606212
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2161995
ClinVar RCV Id: RCV003078854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Ile1402Val
CA218407992
NM_001351297.2:c.4204A>G