Canonical Allele Identifier: PA2827184002
Gene: SV2B HGNC NCBI

Linked Data

ClinVar Variation Id: 161546
ClinVar RCV Id: RCV000149081
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309960.1:p.Arg513Trp
CA174311
NM_001323031.2:c.1537C>T