Canonical Allele Identifier: PA1139695142
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_001295029.1:p.Ala694Pro
CA3385007
NM_001308100.2:c.2080G>C