Allele Registry

Canonical Allele Identifier: PA094718

Gene: SNCA HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.2124464

Score 0.204771048

Score 0.123678296

Score 0.364636138

Score 0.015805231

Score 0.780381656

Score 0.024870508

Score 0.312829389

Score 0.132362054

Score 0.026001915

Score -0.072776458

Score 0.314363579

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000015044

RCV000526380

ClinVar Variation:

14007

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000336.1:p.Ala53Thr	CA257068 NM_000345.4:c.157G>A