Allele Registry

Canonical Allele Identifier: PA127372

Gene: BSG HGNC NCBI

ClinVar RCV:

RCV000019327

ClinVar Variation:

17751

HGVS (amino-acid)	Matching Registered Transcripts
NP_940991.1:p.Glu92Lys	CA127371 NM_198589.3:c.274G>A