Allele Registry

Canonical Allele Identifier: PA171079

Gene: ABCC8 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000144996

RCV000269263

RCV000326750

RCV000388290

RCV000576686

RCV001277184

RCV001533268

RCV001533270

RCV001533271

RCV001533272

RCV002226425

ClinVar Variation:

157699

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Ala1370Ser	CA171077 NM_001287174.3:c.4108G>T