Canonical Allele Identifier: PA916048159
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 328648
ClinVar RCV Id: RCV000525677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357167.1:p.Gln276Glu
CA9322949
NM_001370238.1:c.826C>G