Canonical Allele Identifier: PA112034
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 8468
ClinVar RCV Id: RCV000008989 RCV000540496 RCV000523065 RCV001271089 RCV002336080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Arg155His
CA128983
NM_007126.5:c.464G>A