Canonical Allele Identifier: PA2827740063
Gene: WDPCP HGNC NCBI

Linked Data

ClinVar Variation Id: 336767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340973.1:p.Ser336Leu
CA1682291
NM_001354044.2:c.1007C>T