Canonical Allele Identifier: PA916000688
Gene: SNCA HGNC NCBI

Linked Data

ClinVar Variation Id: 14010
ClinVar RCV Id: RCV000015047 RCV002514100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009292.1:p.Glu46Lys
CA123701
NM_007308.3:c.136G>A