Allele Registry

Canonical Allele Identifier: PA2828569456

Gene: SNCA HGNC NCBI

ClinVar RCV:

RCV000083251

ClinVar Variation:

97000

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362214.1:p.Gly51Asp	CA267501 NM_001375285.1:c.152G>A