Allele Registry

Canonical Allele Identifier: PA096224

Gene: BSND HGNC NCBI

ClinVar RCV:

RCV000004635

RCV002271365

RCV003555916

ClinVar Variation:

4385

HGVS (amino-acid)	Matching Registered Transcripts
NP_476517.1:p.Gly10Ser	CA116809 NM_057176.3:c.28G>A