Canonical Allele Identifier: PA094713
Gene: SNCA HGNC NCBI
ClinVar RCV:
RCV000015045
ClinVar Variation:
14008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000336.1:p.Ala30Pro
CA257069
NM_000345.4:c.88G>C