Canonical Allele Identifier: PA272757
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 160249
ClinVar RCV Id: RCV000147915 RCV000622916 RCV001507436 RCV002274918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Gly494Arg
CA272756
NM_001083961.2:c.1480G>A
CA405437360
NM_001083961.2:c.1480G>C