Canonical Allele Identifier: PA2828569590
Gene: SNCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1051847
ClinVar RCV Id: RCV001359938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362217.1:p.Gln24Arg
CA357715029
NM_001375288.1:c.71A>G