Canonical Allele Identifier: PA2828569600
Gene: SNCA HGNC NCBI

Linked Data

ClinVar Variation Id: 14010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362217.1:p.Glu46Lys
CA123701
NM_001375288.1:c.136G>A