Canonical Allele Identifier: PA112108
Gene: VCP HGNC NCBI
ClinVar RCV:
RCV000023066
ClinVar Variation:
30153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Asp592Asn
CA128985
NM_007126.5:c.1774G>A