Canonical Allele Identifier: PA2742006599
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2577190
ClinVar RCV Id: RCV003324267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Gly589Ser
CA412822646
NM_133499.2:c.1765G>A