Canonical Allele Identifier: PA2828393602
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 328648
ClinVar RCV Id: RCV000525677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357166.1:p.Gln275Glu
CA9322949
NM_001370237.1:c.823C>G