Canonical Allele Identifier: PA2825418819
Gene: WDPCP HGNC NCBI

Linked Data

ClinVar Variation Id: 959729
ClinVar RCV Id: RCV001233129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036157.1:p.Cys184Tyr
CA1682299
NM_001042692.3:c.551G>A