Canonical Allele Identifier: PA2828037778
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_001341857.1:p.Asp547Asn
CA128985
NM_001354928.2:c.1639G>A