Canonical Allele Identifier: PA645377708
Gene: WDPCP HGNC NCBI

Linked Data

ClinVar Variation Id: 336767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056994.3:p.Ser360Leu
CA1682291
NM_015910.7:c.1079C>T