Canonical Allele Identifier: PA2828037360
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 1403085
ClinVar RCV Id: RCV001908873
ClinVar Variation Id: 1496153
ClinVar RCV Id: RCV002015462
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Asn46Lys
CA373293470
NM_001354928.2:c.138C>G
CA373293471
NM_001354928.2:c.138C>A