Canonical Allele Identifier: PA2826922950
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 6078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295038.1:p.Arg217Cys
CA253762
NM_001308109.2:c.649C>T