Canonical Allele Identifier: PA2826922894
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 6078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295037.1:p.Arg315Cys
CA253762
NM_001308108.1:c.943C>T