Allele Registry

Canonical Allele Identifier: PA2826846337

Gene: HELQ HGNC NCBI

ClinVar RCV:

RCV003982500

ClinVar Variation:

3060988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001284688.2:p.Val306Ile	CA2989900 NM_001297759.2:c.916G>A