Canonical Allele Identifier: PA915961381
Gene: WDPCP HGNC NCBI
ClinVar RCV:
RCV000000063
ClinVar Variation:
46
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036157.1:p.Leu49Phe
CA113819
NM_001042692.3:c.147G>C
CA347063316
NM_001042692.3:c.147G>T