Canonical Allele Identifier: PA112073
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 8474
ClinVar RCV Id: RCV000008995 RCV000276565 RCV000639653 RCV003335021 RCV004532314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Arg159His
CA254408
NM_007126.5:c.476G>A