Canonical Allele Identifier: PA318972
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Gly654Glu
CA318970
NM_133499.2:c.1961G>A