Canonical Allele Identifier: PA2580484667
Gene: DHX37 HGNC NCBI

Linked Data

ClinVar Variation Id: 2049434
ClinVar RCV Id: RCV002909712 RCV003926519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116045.2:p.Val999Met
CA6871390
NM_032656.4:c.2995G>A