Canonical Allele Identifier: PA2580484601
Gene: DHX37 HGNC NCBI

Linked Data

ClinVar Variation Id: 2442483
ClinVar RCV Id: RCV003149255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116045.2:p.Tyr452Cys
CA6872062
NM_032656.4:c.1355A>G