Canonical Allele Identifier: PA236155
Gene: VAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 191163
ClinVar RCV Id: RCV000171347 RCV000514140 RCV002254543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004729.1:p.Gly219Val
CA236153
NM_004738.5:c.656G>T