Canonical Allele Identifier: PA916020704
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 350498
ClinVar RCV Id: RCV000298051 RCV000455101 RCV000971881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295029.1:p.Glu756Gln
CA3385033
NM_001308100.2:c.2266G>C