Canonical Allele Identifier: PA2830365335
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 424577
ClinVar RCV Id: RCV000483776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775907.4:p.Arg1391Cys
CA9396499
NM_173636.5:c.4171C>T