Canonical Allele Identifier: PA2573309549
Gene: SYT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1683407
ClinVar RCV Id: RCV002238683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_796376.2:p.Asn368Thr
CA344256073
NM_177402.4:c.1103A>C