Canonical Allele Identifier: PA2825148744
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338249
ClinVar Variation Id: 2829734
ClinVar RCV Id: RCV003686414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Gly1383Arg
CA5902549
NM_000352.6:c.4147G>A
CA379788258
NM_000352.6:c.4147G>C