Canonical Allele Identifier: PA2825827636
Gene: SYT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 816798
ClinVar RCV Id: RCV001007794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129976.1:p.Asp361His
CA344256169
NM_001136504.1:c.1081G>C