Canonical Allele Identifier: PA112016
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 8470
ClinVar RCV Id: RCV000008991 RCV001172005
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Ala232Glu
CA254400
NM_007126.5:c.695C>A