Allele Registry

Canonical Allele Identifier: PA2826614442

Gene: RFXANK HGNC NCBI

ClinVar RCV:

RCV000647944

ClinVar Variation:

538589

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265657.1:p.Ile219Met	CA9322944 NM_001278728.2:c.657C>G