Canonical Allele Identifier: PA891853563
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_036604.2:p.Val432Phe
CA4881086
NM_012472.6:c.1294G>T