Canonical Allele Identifier: PA916071767
Gene: DHX37 HGNC NCBI

Linked Data

ClinVar Variation Id: 735695
ClinVar RCV Id: RCV000911270 RCV003913015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116045.2:p.Ile1147Thr
CA6871189
NM_032656.4:c.3440T>C