Canonical Allele Identifier: PA658807174
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 501096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Pro655Leu
CA412822027
NM_133499.2:c.1964C>T