Canonical Allele Identifier: PA2828037359
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 217877
ClinVar RCV Id: RCV000201935 RCV001271088 RCV001271081 RCV002519583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Asn46Tyr
CA279635
NM_001354928.2:c.136A>T