Canonical Allele Identifier: PA113820
Gene: WDPCP HGNC NCBI
ClinVar RCV:
RCV000000063
ClinVar Variation:
46
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056994.3:p.Leu208Phe
CA113819
NM_015910.7:c.624G>C
CA347063316
NM_015910.7:c.624G>T