Canonical Allele Identifier: PA097472
Gene: VAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 30510
ClinVar RCV Id: RCV000023467 RCV000059634
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Amino-acid Alleles

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