Canonical Allele Identifier: PA2826922832
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 904533
ClinVar RCV Id: RCV001152512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295036.1:p.Ala281Pro
CA3385007
NM_001308107.2:c.841G>C