Canonical Allele Identifier: PA916025029
Gene: WNK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 492932
ClinVar RCV Id: RCV000584086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308228.1:p.Gly884Val
CA399672577
NM_001321299.2:c.2651G>T