Canonical Allele Identifier: PA2829681621
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 501096
ClinVar RCV Id: RCV000591521 RCV002532563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008881.2:p.Pro655Leu
CA412822027
NM_006950.3:c.1964C>T