Canonical Allele Identifier: PA2573096966
Gene: DHX37 HGNC NCBI

Linked Data

ClinVar Variation Id: 1318584
ClinVar RCV Id: RCV001768208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116045.2:p.Gly995Ala
CA387218607
NM_032656.4:c.2984G>C