Canonical Allele Identifier: PA2829681630
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 954219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008881.2:p.Pro658Ser
CA10398340
NM_006950.3:c.1972C>T