Canonical Allele Identifier: PA658659501
Gene: VAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 448853
ClinVar RCV Id: RCV000516581 RCV001143189 RCV002367723 RCV001143188 RCV002254551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004729.1:p.Arg223Trp
CA9924325
NM_004738.5:c.667C>T