Canonical Allele Identifier: PA645508618
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 432305
ClinVar RCV Id: RCV000498690 RCV003766796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Gly128Ala
CA373291969
NM_007126.5:c.383G>C