Canonical Allele Identifier: PA2825516948
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 1370644
ClinVar RCV Id: RCV001864334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Pro1017Arg
CA405449500
NM_001083961.2:c.3050C>G