Canonical Allele Identifier: PA279637
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_009057.1:p.Asn91Tyr
CA279635
NM_007126.5:c.271A>T