Canonical Allele Identifier: PA2828393665
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 538586
ClinVar RCV Id: RCV000647941 RCV002533343
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357167.1:p.Arg111Gln
CA9322681
NM_001370238.1:c.332G>A