Canonical Allele Identifier: PA891857590
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 589838
ClinVar RCV Id: RCV002317551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Pro611Ser
CA412822430
NM_133499.2:c.1831C>T