Canonical Allele Identifier: PA645470656
Gene: DHX37 HGNC NCBI

Linked Data

ClinVar Variation Id: 402138
ClinVar RCV Id: RCV000454335 RCV003333070 RCV003227484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116045.2:p.Arg487His
CA6872021
NM_032656.4:c.1460G>A