Allele Registry

Canonical Allele Identifier: PA2826922950

Gene: SNCAIP HGNC NCBI

ClinVar RCV:

RCV000006451

RCV000314385

RCV000894183

ClinVar Variation:

6078

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