Canonical Allele Identifier: PA2825827642
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_001129976.1:p.Asn368Thr
CA344256073
NM_001136504.1:c.1103A>C