Canonical Allele Identifier: PA112026
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 8469
ClinVar RCV Id: RCV000008990 RCV000372207 RCV000685660 RCV001095424
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Arg155Cys
CA254398
NM_007126.5:c.463C>T