Canonical Allele Identifier: PA112097
Gene: VCP HGNC NCBI
ClinVar RCV:
RCV000008992
ClinVar Variation:
8471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Arg95Gly
CA254402
NM_007126.5:c.283C>G