Canonical Allele Identifier: PA2826922965
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 905317
ClinVar RCV Id: RCV001153784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295038.1:p.Arg327Cys
CA3385048
NM_001308109.2:c.979C>T