Allele Registry

Canonical Allele Identifier: PA2826210294

Gene: VAPB HGNC NCBI

ClinVar Allele:

39467

ClinVar RCV:

RCV000023467

RCV000059634

ClinVar Variation:

30510

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182606.1:p.Thr46Ile	CA219846 NM_001195677.2:c.137C>T