Canonical Allele Identifier: PA645461530
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 328648
ClinVar RCV Id: RCV000525677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003712.1:p.Gln251Glu
CA9322949
NM_003721.4:c.751C>G