Canonical Allele Identifier: PA2580484680
Gene: DHX37 HGNC NCBI
ClinVar RCV:
RCV002939643
ClinVar Variation:
2326239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116045.2:p.Gly1089Ser
CA6871284
NM_032656.4:c.3265G>A