Allele Registry

Canonical Allele Identifier: PA2828393269

Gene: RFXANK HGNC NCBI

ClinVar RCV:

RCV000647944

ClinVar Variation:

538589

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357164.1:p.Ile241Met	CA9322944 NM_001370235.1:c.723C>G