Canonical Allele Identifier: PA318968
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207476
ClinVar RCV Id: RCV000189661 RCV000794382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008881.2:p.Ala648Val
CA318967
NM_006950.3:c.1943C>T