Canonical Allele Identifier: PA2573098628
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1307134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Pro656Leu
CA412822019
NM_133499.2:c.1967C>T