Canonical Allele Identifier: PA2825418827
Gene: WDPCP HGNC NCBI

Linked Data

ClinVar Variation Id: 336767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036157.1:p.Ser201Leu
CA1682291
NM_001042692.3:c.602C>T