Canonical Allele Identifier: PA2499275747
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 1024805
ClinVar RCV Id: RCV001325031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Asn90Asp
CA373293547
NM_007126.5:c.268A>G