Canonical Allele Identifier: PA318971
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207477
ClinVar RCV Id: RCV000189662 RCV000766094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008881.2:p.Gly654Glu
CA318970
NM_006950.3:c.1961G>A