Canonical Allele Identifier: PA2825827631
Gene: SYT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2420137
ClinVar RCV Id: RCV003118662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129976.1:p.Val359Met
CA344256183
NM_001136504.1:c.1075G>A