Canonical Allele Identifier: PA174674
Gene: DHX29 HGNC NCBI

Linked Data

ClinVar Variation Id: 161726
ClinVar RCV Id: RCV000149262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061903.2:p.Glu292Val
CA174673
NM_019030.4:c.875A>T