Canonical Allele Identifier: PA2828037211
Gene: VCP HGNC NCBI
ClinVar RCV:
RCV000023066
ClinVar Variation:
30153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341856.1:p.Asp547Asn
CA128985
NM_001354927.2:c.1639G>A