Canonical Allele Identifier: PA2825516943
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 2484711
ClinVar RCV Id: RCV003217141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Ala1004Pro
CA307841894
NM_001083961.2:c.3010G>C