Canonical Allele Identifier: PA2825827669
Gene: SYT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2635334
ClinVar RCV Id: RCV003393037
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129976.1:p.Glu410Asp
CA344255667
NM_001136504.1:c.1230G>T
CA344255669
NM_001136504.1:c.1230G>C