Canonical Allele Identifier: PA112108
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 30153
ClinVar RCV Id: RCV000023066
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Asp592Asn
CA128985
NM_007126.5:c.1774G>A