Allele Registry

Canonical Allele Identifier: PA110991

Gene: ABCG8 HGNC NCBI

ClinVar Allele:

20009

ClinVar RCV:

RCV000005258

RCV000727975

RCV003407279

ClinVar Variation:

4970

HGVS (amino-acid)	Matching Registered Transcripts
NP_071882.1:p.Arg263Gln	CA253364 NM_022437.3:c.788G>A