Canonical Allele Identifier: PA2827094927
Gene: DNAAF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 568271
ClinVar RCV Id: RCV000688573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308895.1:p.Val292Phe
CA4881086
NM_001321966.2:c.874G>T