Allele Registry

Canonical Allele Identifier: PA2825147679

Gene: ABCC8 HGNC NCBI

ClinVar RCV:

RCV001279204

RCV002480912

ClinVar Variation:

991062

HGVS (amino-acid)	Matching Registered Transcripts
NP_000343.2:p.Trp231Ser	CA379778687 NM_000352.6:c.692G>C