Canonical Allele Identifier: PA2828036991
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 8472
ClinVar RCV Id: RCV000008993 RCV001387337 RCV003137504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341856.1:p.Arg110Pro
CA254404
NM_001354927.2:c.329G>C