Allele Registry

Canonical Allele Identifier: PA645438631

Gene: ABCC8 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

429199

3392678

ClinVar RCV:

RCV000503504

RCV000710389

RCV000763232

RCV001848864

RCV003330733

RCV003470623

RCV004526403

ClinVar Variation:

434045

3233553

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274103.1:p.Gly1479Arg	CA218406864 NM_001287174.3:c.4435G>A CA379783645 NM_001287174.3:c.4435G>C