Canonical Allele Identifier: PA2499301351
Gene: SYT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1192312
ClinVar RCV Id: RCV001553804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_796376.2:p.Asp361_Leu365del
CA2499214410
NM_177402.4:c.1082_1096del