Canonical Allele Identifier: PA267502
Gene: SNCA HGNC NCBI

Linked Data

ClinVar Variation Id: 97000
ClinVar RCV Id: RCV000083251

Amino-acid Alleles

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