Canonical Allele Identifier: PA2573253790
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 1403085
ClinVar RCV Id: RCV001908873
ClinVar Variation Id: 1496153
ClinVar RCV Id: RCV002015462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Asn91Lys
CA373293470
NM_007126.5:c.273C>G
CA373293471
NM_007126.5:c.273C>A