Canonical Allele Identifier: PA2827350878
Gene: DHX30 HGNC NCBI

Linked Data

ClinVar Variation Id: 2444127
ClinVar RCV Id: RCV003152925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317919.1:p.Arg754Pro
CA352590329
NM_001330990.2:c.2261G>C