Allele Registry

Canonical Allele Identifier: PA116808

Gene: BSND HGNC NCBI

ClinVar RCV:

RCV000004634

RCV001057884

RCV001272340

ClinVar Variation:

4384

HGVS (amino-acid)	Matching Registered Transcripts
NP_476517.1:p.Met1Ile