Canonical Allele Identifier: PA318969
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207476
ClinVar RCV Id: RCV000189661 RCV000794382
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Ala648Val
CA318967
NM_133499.2:c.1943C>T