Canonical Allele Identifier: PA105127
Gene: WDR62 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775907.4:p.Trp224Ser
CA251361
NM_173636.5:c.671G>C