Canonical Allele Identifier: PA645389798
Gene: DNAAF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 361901
ClinVar RCV Id: RCV000349818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036604.2:p.Lys393Arg
CA10630278
NM_012472.6:c.1178A>G