Allele Registry

Canonical Allele Identifier: PA916000694

Gene: SNCA HGNC NCBI

ClinVar RCV:

RCV000083251

ClinVar Variation:

97000

HGVS (amino-acid)	Matching Registered Transcripts
NP_009292.1:p.Gly51Asp	CA267501 NM_007308.3:c.152G>A