Allele Registry

Canonical Allele Identifier: PA2580501093

Gene: BSND HGNC NCBI

ClinVar RCV:

RCV002664100

RCV003491264

ClinVar Variation:

2202510

HGVS (amino-acid)	Matching Registered Transcripts
NP_476517.1:p.Arg8Gln	CA871193 NM_057176.3:c.23G>A