Canonical Allele Identifier: PA2580484683
Gene: DHX37 HGNC NCBI

Linked Data

ClinVar Variation Id: 1978724
ClinVar RCV Id: RCV002765886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116045.2:p.Leu1105Phe
CA6871248
NM_032656.4:c.3313C>T