Canonical Allele Identifier: PA2825148742
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 265990
ClinVar RCV Id: RCV000256388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Ser1382Arg
CA10588932
NM_000352.6:c.4146T>G
CA379788276
NM_000352.6:c.4146T>A
CA379788302
NM_000352.6:c.4144A>C