Canonical Allele Identifier: PA658819016
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 532761
ClinVar RCV Id: RCV000639654 RCV000993545 RCV001535609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Ala160Pro
CA373289512
NM_007126.5:c.478G>C