Allele Registry

Canonical Allele Identifier: PA2828393629

Gene: RFXANK HGNC NCBI

ClinVar RCV:

RCV000647950

ClinVar Variation:

538593

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357167.1:p.Ala32Val	CA9322594 NM_001370238.1:c.95C>T