Canonical Allele Identifier: PA2826313338
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 350500
ClinVar RCV Id: RCV000262821 RCV004021978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229864.1:p.Ala348Thr
CA3385036
NM_001242935.3:c.1042G>A