Canonical Allele Identifier: PA2573098627
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1320752
ClinVar RCV Id: RCV001776731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Gly596Val
CA412822574
NM_133499.2:c.1787G>T