Canonical Allele Identifier: PA2828569470
Gene: SNCA HGNC NCBI
ClinVar RCV:
RCV002017665
ClinVar Variation:
1509118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362214.1:p.Glu83Gln
CA357714631
NM_001375285.1:c.247G>C