Canonical Allele Identifier: PA1139752238
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 962183
ClinVar RCV Id: RCV001235992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Ala523Val
CA412823287
NM_133499.2:c.1568C>T