Allele Registry

Canonical Allele Identifier: PA111079

Gene: ABCG8 HGNC NCBI

ClinVar RCV:

RCV000005262

ClinVar Variation:

4974

HGVS (amino-acid)	Matching Registered Transcripts
NP_071882.1:p.Pro231Thr	CA253369 NM_022437.3:c.691C>A