Allele Registry

Canonical Allele Identifier: PA2826922770

Gene: SNCAIP HGNC NCBI

ClinVar RCV:

RCV000006451

RCV000314385

RCV000894183

ClinVar Variation:

6078

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295035.1:p.Arg253Cys	CA253762 NM_001308106.1:c.757C>T