Allele Registry

Canonical Allele Identifier: PA916068448

Gene: RFXANK HGNC NCBI

ClinVar RCV:

RCV000647950

ClinVar Variation:

538593

HGVS (amino-acid)	Matching Registered Transcripts
NP_604389.1:p.Ala32Val	CA9322594 NM_134440.3:c.95C>T