Canonical Allele Identifier: PA2830248577
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 328648
ClinVar RCV Id: RCV000525677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_604389.1:p.Gln228Glu
CA9322949
NM_134440.3:c.682C>G