Canonical Allele Identifier: PA251362
Gene: WDR62 HGNC NCBI
ClinVar RCV:
RCV000000059
ClinVar Variation:
42
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Trp224Ser
CA251361
NM_001083961.2:c.671G>C