Canonical Allele Identifier: PA2499275746
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 1010487
ClinVar RCV Id: RCV001308126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Arg89Trp
CA373293559
NM_007126.5:c.265C>T