Canonical Allele Identifier: PA2828037135
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 464105
ClinVar RCV Id: RCV000534353 RCV001579523 RCV004537963 RCV002350262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341856.1:p.Asn356Ser
CA5039291
NM_001354927.2:c.1067A>G