Canonical Allele Identifier: PA2828569553
Gene: SNCA HGNC NCBI

Linked Data

ClinVar Variation Id: 162095
ClinVar RCV Id: RCV000149507 RCV000344706 RCV001301465 RCV002307408 RCV002498683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362216.1:p.His50Gln
CA273048
NM_001375287.1:c.150T>G
CA357714845
NM_001375287.1:c.150T>A