Canonical Allele Identifier: PA116805
Gene: BSND HGNC NCBI

Linked Data

ClinVar Variation Id: 4380
ClinVar RCV Id: RCV000004630 RCV001579751
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_476517.1:p.Met1Leu