Canonical Allele Identifier: PA2828569554
Gene: SNCA HGNC NCBI

Linked Data

ClinVar Variation Id: 97000
ClinVar RCV Id: RCV000083251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362216.1:p.Gly51Asp
CA267501
NM_001375287.1:c.152G>A