This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2828569444
Gene: SNCA HGNC NCBI
ClinVar RCV:
RCV000015045
ClinVar Variation:
14008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362214.1:p.Ala30Pro
CA257069
NM_001375285.1:c.88G>C