Canonical Allele Identifier: PA658661805
Gene: WDR48 HGNC NCBI

Linked Data

ClinVar Variation Id: 424665
ClinVar RCV Id: RCV000516121 RCV000762109 RCV003915340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065890.1:p.Ser94Ala
CA2322939
NM_020839.4:c.280T>G