Allele Registry

Canonical Allele Identifier: PA267502

Gene: SNCA HGNC NCBI

ClinVar RCV:

RCV000083251

ClinVar Variation:

97000

HGVS (amino-acid)	Matching Registered Transcripts
NP_000336.1:p.Gly51Asp	CA267501 NM_000345.4:c.152G>A