Canonical Allele Identifier: PA2741999325
Gene: DHX37 HGNC NCBI

Linked Data

ClinVar Variation Id: 2903286
ClinVar RCV Id: RCV003726652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116045.2:p.Met1143Val
CA6871194
NM_032656.4:c.3427A>G