Canonical Allele Identifier: PA2826922901
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2233119
ClinVar RCV Id: RCV004094133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295037.1:p.Ala390Val
CA125942576
NM_001308108.1:c.1169C>T