Canonical Allele Identifier: PA1139722065
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 940463
ClinVar RCV Id: RCV001210057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Ser748Cys
CA373269685
NM_007126.5:c.2242A>T