Canonical Allele Identifier: PA113822
Gene: WDPCP HGNC NCBI
ClinVar RCV:
RCV000000064
ClinVar Variation:
47
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056994.3:p.Arg55Lys
CA113821
NM_015910.7:c.164G>A