Canonical Allele Identifier: PA2741985144
Gene: DHX58 HGNC NCBI

Linked Data

ClinVar Variation Id: 2548245
ClinVar RCV Id: RCV004319539
ClinVar Variation Id: 3082335
ClinVar RCV Id: RCV004373674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077024.2:p.His314Gln
CA399541569
NM_024119.3:c.942C>G
CA399541571
NM_024119.3:c.942C>A