Allele Registry

Canonical Allele Identifier: PA2828393598

Gene: RFXANK HGNC NCBI

ClinVar RCV:

RCV000647944

ClinVar Variation:

538589

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357166.1:p.Ile266Met	CA9322944 NM_001370237.1:c.798C>G