Allele Registry

Canonical Allele Identifier: PA097472

Gene: VAPB HGNC NCBI

ClinVar Allele:

39467

ClinVar RCV:

RCV000023467

RCV000059634

ClinVar Variation:

30510

HGVS (amino-acid)	Matching Registered Transcripts
NP_004729.1:p.Thr46Ile	CA219846 NM_004738.5:c.137C>T