Allele Registry

Canonical Allele Identifier: PA2827153087

Gene: BSG HGNC NCBI

ClinVar Allele:

32790

ClinVar RCV:

RCV000019327

ClinVar Variation:

17751

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309172.1:p.Glu92Lys	CA127371 NM_001322243.2:c.274G>A