Canonical Allele Identifier: PA2580484668
Gene: DHX37 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116045.2:p.Lys1016Glu
CA6871381
NM_032656.4:c.3046A>G