Allele Registry

Canonical Allele Identifier: PA096233

Gene: BSND HGNC NCBI

ClinVar RCV:

RCV000004637

RCV001058739

RCV001826415

RCV003934797

ClinVar Variation:

4387

HGVS (amino-acid)	Matching Registered Transcripts
NP_476517.1:p.Gly47Arg	CA116811 NM_057176.3:c.139G>A CA340470791 NM_057176.3:c.139G>C