Canonical Allele Identifier: PA118367
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 6600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003712.1:p.Asp121Val
CA118365
NM_003721.4:c.362A>T