Allele Registry

Canonical Allele Identifier: PA121329

Gene: PHF6 HGNC NCBI

ClinVar RCV:

RCV000011815

ClinVar Variation:

11066

HGVS (amino-acid)	Matching Registered Transcripts
NP_115711.2:p.Cys45Tyr	CA121326 NM_032335.3:c.134G>A