Canonical Allele Identifier: PA645485023
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 424577
ClinVar RCV Id: RCV000483776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Arg1396Cys
CA9396499
NM_001083961.2:c.4186C>T