Canonical Allele Identifier: PA2826922964
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2277017
ClinVar RCV Id: RCV004124826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295038.1:p.Leu322Met
CA3385046
NM_001308109.2:c.964T>A