Canonical Allele Identifier: PA2828037671
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 464105
ClinVar RCV Id: RCV000534353 RCV001579523 RCV004537963 RCV002350262
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Asn356Ser
CA5039291
NM_001354928.2:c.1067A>G