Canonical Allele Identifier: PA2828036888
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 280124
ClinVar RCV Id: RCV000280148 RCV000761344 RCV001215048 RCV001391611 RCV001095441 RCV002436094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341856.1:p.Arg50Cys
CA10603200
NM_001354927.2:c.148C>T