Canonical Allele Identifier: PA645484739
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 328921
ClinVar RCV Id: RCV000309409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Pro1054Arg
CA9396172
NM_001083961.2:c.3161C>G