Allele Registry

Canonical Allele Identifier: PA645440885

Gene: ABCG8 HGNC NCBI

ClinVar Variation Id: 336084

HGVS (amino-acid)	Matching Registered Transcripts
NP_071882.1:p.Pro523Leu	CA1637546 NM_022437.3:c.1568C>T