Allele Registry

Canonical Allele Identifier: PA658659501

Gene: VAPB HGNC NCBI

ClinVar Allele:

442305

ClinVar RCV:

RCV000516581

RCV001143188

RCV001143189

RCV002254551

RCV002367723

ClinVar Variation:

448853

HGVS (amino-acid)	Matching Registered Transcripts
NP_004729.1:p.Arg223Trp	CA9924325 NM_004738.5:c.667C>T