Canonical Allele Identifier: PA2827184069
Gene: SV2B HGNC NCBI

Linked Data

ClinVar Variation Id: 161546
ClinVar RCV Id: RCV000149081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309962.1:p.Arg402Trp
CA174311
NM_001323033.3:c.1204C>T