Canonical Allele Identifier: PA916020706
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 350500
ClinVar RCV Id: RCV000262821 RCV004021978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295029.1:p.Ala761Thr
CA3385036
NM_001308100.2:c.2281G>A