Allele Registry

Canonical Allele Identifier: PA2828569502

Gene: SNCA HGNC NCBI

ClinVar RCV:

RCV000015047

RCV002514100

ClinVar Variation:

14010

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362215.1:p.Glu46Lys	CA123701 NM_001375286.1:c.136G>A