Canonical Allele Identifier: PA2828569508
Gene: SNCA HGNC NCBI

Linked Data

ClinVar Variation Id: 14007
ClinVar RCV Id: RCV000015044 RCV000526380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362215.1:p.Ala53Thr
CA257068
NM_001375286.1:c.157G>A