Canonical Allele Identifier: PA2825418951
Gene: WDPCP HGNC NCBI

Linked Data

ClinVar Variation Id: 1363607
ClinVar RCV Id: RCV001904997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036157.1:p.Arg441Cys
CA1682111
NM_001042692.3:c.1321C>T