Canonical Allele Identifier: PA2828037356
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 1024805
ClinVar RCV Id: RCV001325031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Asn45Asp
CA373293547
NM_001354928.2:c.133A>G