Allele Registry

Canonical Allele Identifier: PA916000695

Gene: SNCA HGNC NCBI

ClinVar RCV:

RCV000015044

RCV000526380

ClinVar Variation:

14007

HGVS (amino-acid)	Matching Registered Transcripts
NP_009292.1:p.Ala53Thr	CA257068 NM_007308.3:c.157G>A