Canonical Allele Identifier: PA645497200
Gene: SYT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373966
ClinVar RCV Id: RCV000415021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_796376.2:p.Tyr362_Asp363del
CA16043364
NM_177402.4:c.1084_1089del