Canonical Allele Identifier: PA2826922705
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2590935
ClinVar RCV Id: RCV004341433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295034.1:p.Arg546Trp
CA3384993
NM_001308105.1:c.1636C>T