Canonical Allele Identifier: PA207774
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 212607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Arg1396His
CA207773
NM_001083961.2:c.4187G>A