Canonical Allele Identifier: PA2825827647
Gene: SYT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1192311
ClinVar RCV Id: RCV001553803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129976.1:p.Ile371Lys
CA344256034
NM_001136504.1:c.1112T>A