Allele Registry

Canonical Allele Identifier: PA253763

Gene: SNCAIP HGNC NCBI

ClinVar RCV:

RCV000006451

RCV000314385

RCV000894183

ClinVar Variation:

6078

HGVS (amino-acid)	Matching Registered Transcripts
NP_005451.2:p.Arg621Cys	CA253762 NM_005460.4:c.1861C>T