Canonical Allele Identifier: PA916037033
Gene: WDPCP HGNC NCBI

Linked Data

ClinVar Variation Id: 336770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340973.1:p.Asp4Val
CA1682617
NM_001354044.2:c.11A>T