Canonical Allele Identifier: PA2827740041
Gene: WDPCP HGNC NCBI

Linked Data

ClinVar Variation Id: 1042588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340973.1:p.Ala316Ser
CA1682300
NM_001354044.2:c.946G>T