Canonical Allele Identifier: PA2580484597
Gene: DHX37 HGNC NCBI

Linked Data

ClinVar Variation Id: 2057858
ClinVar RCV Id: RCV002914967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116045.2:p.Pro426Leu
CA6872127
NM_032656.4:c.1277C>T