Canonical Allele Identifier: PA2825827637
Gene: SYT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373966
ClinVar RCV Id: RCV000415021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129976.1:p.Tyr362_Asp363del
CA16043364
NM_001136504.1:c.1084_1089del