Allele Registry

Canonical Allele Identifier: PA113493

Gene: PHF6 HGNC NCBI

ClinVar RCV:

RCV000011816

ClinVar Variation:

11067

HGVS (amino-acid)	Matching Registered Transcripts
NP_001015877.1:p.His229Arg	CA121330 NM_001015877.2:c.686A>G