Allele Registry

Canonical Allele Identifier: PA2741978332

Gene: ABCG8 HGNC NCBI

ClinVar RCV:

RCV003493257

ClinVar Variation:

2690820

HGVS (amino-acid)	Matching Registered Transcripts
NP_071882.1:p.Thr400Met	CA1637336 NM_022437.3:c.1199C>T