Canonical Allele Identifier: PA916020700
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 350488
ClinVar RCV Id: RCV000323147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295029.1:p.Ser269Leu
CA3384686
NM_001308100.2:c.806C>T