Canonical Allele Identifier: PA658820175
Gene: VAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 534269
ClinVar RCV Id: RCV002254560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004729.1:p.Ala65Val
CA409442780
NM_004738.5:c.194C>T