Canonical Allele Identifier: PA2825148923
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 434043
ClinVar Variation Id: 554959
ClinVar RCV Id: RCV000670686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Lys1521Asn
CA5902427
NM_000352.6:c.4563G>T
CA379782126
NM_000352.6:c.4563G>C