Allele Registry

Canonical Allele Identifier: PA2829340117

Gene: BSG HGNC NCBI

ClinVar Allele:

32790

ClinVar RCV:

RCV000019327

ClinVar Variation:

17751

HGVS (amino-acid)	Matching Registered Transcripts
NP_001719.2:p.Glu208Lys	CA127371 NM_001728.4:c.622G>A