Canonical Allele Identifier: PA2828037280
Gene: VCP HGNC NCBI
ClinVar RCV:
RCV001210057
ClinVar Variation:
940463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341856.1:p.Ser703Cys
CA373269685
NM_001354927.2:c.2107A>T