Allele Registry

Canonical Allele Identifier: PA2827606161

Gene: ABCC8 HGNC NCBI

ClinVar Allele:

3167202

ClinVar RCV:

RCV003851783

ClinVar Variation:

2999152

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338226.1:p.Ala1368Thr	CA5902584 NM_001351297.2:c.4102G>A