Allele Registry

Canonical Allele Identifier: PA916048158

Gene: RFXANK HGNC NCBI

ClinVar RCV:

RCV000647944

ClinVar Variation:

538589

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357167.1:p.Ile267Met	CA9322944 NM_001370238.1:c.801C>G